EP2536708A2 - Modulateurs du récepteur des androgènes et leurs utilisations - Google Patents

Modulateurs du récepteur des androgènes et leurs utilisations

Info

Publication number
EP2536708A2
EP2536708A2 EP11745183A EP11745183A EP2536708A2 EP 2536708 A2 EP2536708 A2 EP 2536708A2 EP 11745183 A EP11745183 A EP 11745183A EP 11745183 A EP11745183 A EP 11745183A EP 2536708 A2 EP2536708 A2 EP 2536708A2
Authority
EP
European Patent Office
Prior art keywords
substituted
unsubstituted
oxo
diazaspiro
thioxo
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP11745183A
Other languages
German (de)
English (en)
Other versions
EP2536708A4 (fr
Inventor
Nicholas D. Smith
Celine Bonnefous
Jackaline D. Julien
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Aragon Pharmaceuticals Inc
Original Assignee
Aragon Pharmaceuticals Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Aragon Pharmaceuticals Inc filed Critical Aragon Pharmaceuticals Inc
Priority to PL16184263T priority Critical patent/PL3124481T3/pl
Priority to EP18161153.4A priority patent/EP3357917A1/fr
Priority to EP16184263.8A priority patent/EP3124481B1/fr
Priority to EP14188300.9A priority patent/EP2824102B1/fr
Publication of EP2536708A2 publication Critical patent/EP2536708A2/fr
Publication of EP2536708A4 publication Critical patent/EP2536708A4/fr
Priority to CY20181100592T priority patent/CY1120297T1/el
Withdrawn legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4164—1,3-Diazoles
    • A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
    • A—HUMAN NECESSITIES
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    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • A—HUMAN NECESSITIES
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    • A61K31/33—Heterocyclic compounds
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    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
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    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
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    • A—HUMAN NECESSITIES
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    • A61K31/4965—Non-condensed pyrazines
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    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/50—Pyridazines; Hydrogenated pyridazines
    • A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
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    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
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    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/513—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
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    • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
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    • A61K31/635—Compounds containing para-N-benzenesulfonyl-N-groups, e.g. sulfanilamide, p-nitrobenzenesulfonyl hydrazide having a heterocyclic ring, e.g. sulfadiazine
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    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems

Definitions

  • Described herein are compounds, including pharmaceutically acceptable salts, solvates, metabolites, prodrugs thereof, methods of making such compounds, pharmaceutical compositions comprising such compounds, and methods of using such compounds to treat, prevent or diagnose diseases or conditions that are androgen receptor dependent or androgen receptor mediated.
  • the androgen receptor (“AR”) is a ligand-activated transcriptional regulatory protein that mediates induction of a variety of biological effects through its interaction with with endogenous androgens.
  • Endogenous androgens include steroids such as testosterone and dihydrotestosterone.
  • Testosterone is converted to dihydrotestosterone by the enzyme 5 alpha- reductase in many tissues.
  • compounds of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) and (X) are useful for the treatment of benign prostate hyperplasia, hirsutism, acne, adenomas and neoplasies of the prostate, benign or malignant tumor cells containing the androgen receptor, hyperpilosity, seborrhea, endometriosis, polycystic ovary syndrome, androgenic alopecia, hypogonadism, osteoporosis, suppression of spermatogenesis, libido, cachexia, anorexia, androgen supplementation for age related decreased testosterone levels, prostate cancer, breast cancer, endometrial cancer, uterine cancer, hot flashes, and Kennedy's disease muscle atrophy and weakness, skin atrophy, bone loss, anemia,
  • a compound of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X) is used in the treatment of prostate cancer.
  • a compound of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X) are used in the treatment of hormone-sensitive prostate cancer.
  • a compound of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X) is used in the treatment of hormone refractory prostate cancer.
  • compounds of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) and (X) are androgen receptor modulators.
  • (VII) , (VIII), (Villa), (IX), (IXa) or (X) is an androgen receptor antagonist, an androgen receptor inverse agonist, an androgen receptor degrader, an androgen receptor trafficking modulator and/or an androgen receptor DNA-binding inhibitor.
  • the compoud of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X) is an androgen receptor antagonist.
  • the compoud of Formula (I), (II), (III), (IV), (V), (VI), (VII), (VIII), (IX) or (X) is an androgen receptor inverse agonist. In some embodiments, the compoud of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X) is an androgen receptor degrader.
  • the compoud of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X) is an androgen receptor trafficking modulator.
  • the compoud of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X) is an androgen receptor DNA-binding inhibitor.
  • ring A is monocyclic heteroaryl, bicyclic heteroaryl, or naphthyl
  • n 0, 1, 2, 3 or 4;
  • each R A is independently selected from H, halogen, -CN, -N0 2 , -OH, -OR 9 , -SR 9 , -
  • each R 1 is independently selected from H, -OH, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 alkoxy, and substituted or unsubstituted C
  • R 1 are taken together with the carbon atom to which they are attached to form a substituted or unsubstituted C3-Ciocycloalkyl or a substituted or unsubstituted C 2 -
  • ring B is phenyl, naphthyl, monocyclic heteroaryl, or bicyclic heteroaryl;
  • n 0, 1, 2, 3 or 4;
  • each R 4 is independently selected from H, halogen, -CN, -N0 2 , -OH, -OR 9 , -SR 9 , -
  • R 5 is substituted or unsubstituted C2-Cioalkyl, substituted or unsubstituted C 2 -
  • Ciofluoroalkyl substituted or unsubstituted C 2 -Ci 0 alkoxy, substituted or unsubstituted C2-Ciofluoroalkoxy, substituted or unsubstituted C2-Cioheteroalkyl, substituted or unsubstituted C 2 -Ci 0 heterofluoroalkyl, or -I ⁇ -IAR 6 ;
  • L 2 is substituted or unsubstituted Ci-C 6 alkylene, substituted or unsubstituted C
  • each R 9 is independently selected from H, substituted or unsubstituted Ci-C 6 alkyl,
  • Ci-C 6 heteroalkyl substituted or unsubstituted Ci- C 6 fluoroalkyl, substituted or unsubstituted C 3 -Ciocycloalkyl, substituted or
  • R 10 is substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 heteroalkyl, substituted or unsubstituted Ci-C 6 fiuoroaikyl, a substituted or unsubstituted C 3 - Ciocycloalkyl, a substituted or unsubstituted C 2 -Ci 0 heterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted benzyl, a substituted or unsubstituted heteroaryl, -Ci-C 4 alkylene-(substituted or unsubstituted C 3 -Ci 0 cycloalkyl), -C C 4 alkylene-(substituted or unsubstituted C 2 -Ci 0 heterocycloalkyl), -Ci-C 4 alkylene- (substituted or unsubstitute
  • R 11 is H or C C 4 alkyl.
  • substituents are selected from among from a subset of the listed alternatives.
  • both R 1 are taken together with the carbon atom to which they are attached to form a substituted or unsubstituted C 3 - Ciocycloalkyl.
  • both R 1 are taken together with the carbon atom to which they are attached to form a substituted or unsubstituted cyclopropyl, cyclobutyl, cyclopentyl, or cyclcohexyl.
  • each R 1 is independently selected from H, -OH, Ci-C 6 alkyl, and Ci-C 6 fluoroalkyl.
  • each R 1 is independently selected from H, -CH 3 and -CF 3 .
  • ring A is C-linked monocyclic heteroaryl, C-linked bicyclic heteroaryl, or naphthyl.
  • both R 1 are taken together with the carbon atom to which they are attached to form a cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl;
  • ring A is N- containing monocyclic heteroaryl selected from pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, triazinyl, pyrrolyl, thiazolyl, oxazolyl, isoxazolyl, oxadiazolyl, imidazolyl, pyrazolyl, isothiazolyl, triazolyl, and tetrazolyl.
  • ring A is pyridinyl, pyrimidinyl, pyridazinyl, or pyrazinyl. In some embodiments, ring A is pyridinyl.
  • both R 1 are taken together with the carbon atom to which they are attached to form a cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl;
  • ring A is N- containing bicyclic heteroaryl selected from quinolinyl, isoquinolinyl, quinazolinyl, quinoxalinyl, naphthyridinyl, indolyl, indazolyl, benzoxazolyl, benzisoxazolyl, benzofuranyl, benzothienyl, benzothiazolyl, benzimidazolyl, purinyl, cinnolinyl, phthalazinyl, pteridinyl, pyridopyrimidinyl, pyrazolopyrimidinyl, azaindolyl, pyrazolopyridinyl, thiazolopyrimidinyl, triazolopyridazin
  • ring A is N-containing bicyclic heteroaryl selected from quinolinyl, isoquinolinyl, quinazolinyl, quinoxalinyl, pyridopyrimidinyl, pyrazolopyrimidinyl, triazolopyridazinyl, and pyrrolopyrimidinyl.
  • ring A is [l ,2,4]triazolo[4,3-b]pyridazinyl.
  • ring B is phenyl or monocyclic heteroaryl; each R 4 is independently selected from H, halogen, -CN, -N0 2 , -OH, substituted or unsubstituted Ci- C 6 alkyl, substituted or unsubstituted Ci-C 6 fluoroalkyl, substituted or unsubstituted C C 6 fluoroalkoxy, substituted or unsubstituted Ci-C 6 alkoxy, and substituted or unsubstituted C Ceheteroalkyl; R 5 is substituted or unsubstituted C 2 -Cioalkyl, substituted or unsubstituted C 2 - Ciofluoroalkyl, substituted or unsubstituted C 2 -Cioalkoxy, substituted or unsubstituted C 2 - Ciofluoroalkoxy, substituted or unsubstituted C 2 -Ci 0 heteroalkyl, substituted or unsubstituted
  • ring B is phenyl or monocyclic heteroaryl; each R 4 is independently selected from H, halogen, -CN, -N0 2 , -OH, substituted or unsubstituted Ci- C 4 alkyl, substituted or unsubstituted Ci-C 4 fluoroalkyl, substituted or unsubstituted C
  • L 2 is substituted or unsubstituted Ci-C 6 alkylene;
  • R 6 is substituted or unsubstituted C 3 -Ci 0 cycloalkyl, substituted or unsubstituted C 2 -Ci 0 heterocycloalkyl, substituted or unsubstituted monocyclic heteroaryl, substituted or unsubstituted bicyclic heteroaryl, substituted or unsubstituted phenyl, or substituted or unsubstituted naphthyl.
  • L 2 is substituted or unsubstituted Ci-C 6 alkylene;
  • each R 9 is independently selected from H, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci- C 6 fluoroalkyl, -Ci-C 4 alkylene-(substituted or unsubstituted C 3 -Ci 0 cycloalkyl), -CrQalkylene- (substituted or unsubstituted C2-Cioheterocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted aryl), and -Ci-C
  • ring A is monocyclic heteroaryl, bicyclic heteroaryl, or naphthyl
  • n 1, 2, 3 or 4;
  • both R 1 are taken together with the carbon atom to which they are attached to form a
  • each R 1 is independently selected from H, -OH, Ci-C 6 alkyl, Ci-C 6 alkoxy, and Cr
  • X is S or O
  • ring B is phenyl, naphthyl, monocyclic heteroaryl, or bicyclic heteroaryl;
  • n 0, 1, 2, 3 or 4; each R 4 is independently selected from H, halogen, -CN, -N0 2 , -OH, -OR 9 , -SR 9 , -
  • R 5 is - ⁇ ⁇ ⁇ -L'-R 7 ;
  • L 2 is Ci-C 6 alkylene, Ci-C 6 fluoroaikylene or Ci-C 6 heteroalkylene;
  • Ci-C 6 fluoroalkyl Ci-C 6 heteroalkyl, substituted or unsubstituted C 3 - Ciocycloalkyl, substituted or unsubstituted C 2 -Ci 0 heterocycloalkyl, substituted or unsubstituted monocyclic heteroaryl, substituted or unsubstituted bicyclic heteroaryl, substituted or unsubstituted phenyl, or substituted or unsubstituted naphthyl;
  • R 7 is substituted or unsubstituted monocyclic C 2 -C 6 heterocycloalkyl, or substituted or unsubstituted monocyclic heteroaryl;
  • each R 9 is independently selected from H, Ci-C 6 alkyl, Ci-C 6 heteroalkyl, Ci-C 6 fiuoroaikyl, substituted or unsubstituted C 3 -C 6 Cycloalkyl, substituted or unsubstituted C 2 - Cioheterocycloalkyl, substituted or unsubstituted phenyl, substituted or unsubstituted monocyclic heteroaryl, -Ci-C 4 alkylene-(substituted or unsubstituted C 3 -C 6 cycloalkyl), - Ci-C 4 alkylene-(substituted or unsubstituted monocyclic C 2 -C 6 heterocycloalkyl), -Cr C 4 alkylene-(substituted or unsubstituted phenyl), and -Ci-C 4 alkylene-(substituted or unsubstituted monocyclic heteroaryl); or
  • R 10 is Ci-C 6 alkyl, Ci-C 6 heteroalkyl, Ci-C 6 fiuoroalkyl, a substituted or unsubstituted C3- C 6 cycloalkyl, a substituted or unsubstituted monocyclic C 2 -C 6 heterocycloalkyl, a substituted or unsubstituted phenyl, a substituted or unsubstituted benzyl, a substituted or unsubstituted monocyclic heteroaryl, -Ci-C 4 alkylene-(substituted or unsubstituted C 3 C 6 cycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted monocyclic C 2 - C 6 heterocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted phenyl), or -C C 4 alkylene-(substituted or un
  • R 11 is H or Ci-C 4 alkyl.
  • both R 1 are taken together with the carbon atom to which they are attached to form a substituted or unsubstituted C 3 -C 6 Cycloalkyl;
  • X is S;
  • ring B is phenyl or monocyclic heteroaryl.
  • both R 1 are taken together with the carbon atom to which they are attached to form a cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl; ring A is pyridinyl, pyrimidinyl, pyridazinyl, or pyrazinyl.
  • ring B is phenyl;
  • R 5 is -L'-lAR 6 ;
  • L 2 is C C 6 alkylene, Ci-C 6 fluoroalkylene or C C 6 heteroalkylene;
  • L 2 is C C 6 alkylene;
  • R 6 is substituted or unsubstituted C 3 -C 6 cycloalkyl, substituted or unsubstituted C2-C6heterocycloalkyl, substituted or unsubstituted monocyclic heteroaryl, or substituted or unsubstituted phenyl.
  • L 2 is Ci-C 6 alkylene; R 6 is a substituted or unsubstituted C 2 - C 6 heterocycloalkyl.
  • ring B is phenyl; each R 4 is independently selected from H, halogen, -CN, -N0 2 , -OH, Ci-C 4 alkyl, Ci-C 4 fluoroalkyl, Ci-C 4 fluoroalkoxy, and C C 4 alkoxy;
  • R 5 is -L'-R 7 ;
  • R 5 is -L'-R 7 ;
  • R 7 is substituted or unsubstituted monocyclic C 2 - C6heterocycloalkyl, or substituted or unsubstituted monocyclic heteroaryl.
  • R 5 is -L'-R 7 ;
  • R 7 is substituted or unsubstituted monocyclic heteroaryl.
  • the compound of Formula (I) or Formula (la) has the structure of Formula (II):
  • the compound of Formula (la) has the structure of Formula (II):
  • n 2;
  • R A is H, halogen, -OH, C C 6 alkyl, CrC 6 fluoroalkyl, Ci-C 6 fluoroalkoxy, or Ci-C 6 alkoxy;
  • n 0 or 1 ;
  • each R 4 is independently selected from H, halogen, -CN, -N0 2 , -OH, Ci-C 6 alkyl, C
  • R 5 is -L'-LAR 6 or -L'-R 7 ;
  • L 2 is Ci-C 6 alkylene, Ci-C 6 fluoroalkylene or Ci-C 6 heteroalkylene;
  • R 7 is substituted or unsubstituted monocyclic C 2 -C 6 heterocycloalkyl, or substituted or unsubstituted monoc tract heteroaryl.
  • one R A is -CN and the other R A is
  • R 4 is independently selected from H, halogen, -OH, Ci-C 4 alkyl, Ci-C 4 fluoroalkyl, Ci-C 4 fluoroalkoxy, or Ci-C 4 alkoxy; each R 4 is independently selected from H, halogen, -OH, Ci-C 4 alkyl, Ci-C 4 fluoroalkyl, Ci-C 4 fluoroalkoxy, and Ci-C 4 alkoxy;
  • R 5 is -L L -L 2 -R 6 or -L'-R 7 ;
  • L 2 is C
  • a compound of Formula (I) or a pharmaceutically acceptable salt, solvate, N-oxide, metabolite or prodrug thereof:
  • ring A is bicyclic heteroaryl, or naphthyl
  • n 0, 1, 2, or 3;
  • each R A is independently selected from H, halogen, -CN, -N0 2 , -OH, -OR 9 , -SR 9 , -
  • each R 1 is independently selected from H, -OH, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 alkoxy, and substituted or unsubstituted Ci-
  • R 1 are taken together with the carbon atom to which they are attached to form a substituted or unsubstituted C3-Ciocycloalkyl or a substituted or unsubstituted C 2 - Cioheterocycloalkyl;
  • ring B is phenyl, naphthyl, monocyclic heteroaryl, or bicyclic heteroaryl;
  • n 0, 1, or 2;
  • each R 4 is independently selected from H, halogen, -CN, -N0 2 , -OH, -OR 9 , -SR 9 , -
  • L 2 is substituted or unsubstituted Ci-C 6 alkylene, substituted or unsubstituted C
  • each R 9 is independently selected from H, substituted or unsubstituted Ci-C 6 alkyl,
  • C 6 fluoroalkyl a substituted or unsubstituted C 3 -Ciocycloalkyl, a substituted or unsubstituted C 2 -Ci 0 heterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted heteroaryl, -Ci-C4alkylene-(substituted or unsubstituted C 3 - Ciocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted C 2 -Ci 0 heterocycloalkyl), - Ci-C 4 alkylene-(substituted or unsubstituted aryl), and -Ci-C 4 alkylene-(substituted or unsubstituted heteroaryl); or
  • R 10 is substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 heteroalkyl, substituted or unsubstituted Ci-C 6 fiuoroaikyl, a substituted or unsubstituted C 3 - Ciocycloalkyl, a substituted or unsubstituted C 2 -Ci 0 heterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted heteroaryl, -Ci-C 4 alkylene-(substituted or unsubstituted C 3 -Ci 0 cycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted C 2 - Cioheterocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted aryl), or -C r C 4 al
  • R 11 is H or Ci-C 4 alkyl.
  • ring A is selected from quinolinyl, isoquinolinyl, quinazolinyl, quinoxalinyl, naphthyridinyl, indolyl, indazolyl, benzoxazolyl, benzisoxazolyl, benzofuranyl, benzothienyl, benzothiazolyl, benzimidazolyl, purinyl, cinnolinyl, phthalazinyl, pteridinyl, pyridopyrimidinyl, pyrazolopynmidinyl, azaindolyl, pyrazolopyridinyl, thiazolopyrimidinyl, triazolopyridazinyl, thiazolopyridinyl, pyridothienyl, pyrimidiothienyl, pyrrolopyrimidinyl and naphthyl.
  • ring A is selected from quinolinyl, isoquinolinyl, quinazolinyl, quinoxalinyl, pyridopyrimidinyl, pyrazolopyrimidinyl, triazolopyridazinyl, pyrrolopyrimidinyl, and napthyl.
  • ring A is [l,2,4]triazolo[4,3-b]pyridazinyl.
  • ring A is a 5-membered heteroaryl
  • n 0, 1, 2, or 3;
  • each R A is independently selected from H, halogen, -CN, -N0 2 , -OH, -OR 9 , -SR 9 , -
  • each R 1 is independently selected from H, -OH, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 alkoxy, and substituted or unsubstituted C
  • R 1 are taken together with the carbon atom to which they are attached to form a substituted or unsubstituted C3-Ciocycloalkyl or a substituted or unsubstituted C 2 - Cioheterocycloalkyl;
  • ring B is phenyl, naphthyl, monocyclic heteroaryl, or bicyclic heteroaryl;
  • n 0, 1, or 2;
  • each R 4 is independently selected from H, halogen, -CN, -N0 2 , -OH, -OR 9 , -SR 9 , -
  • L 2 is substituted or unsubstituted Ci-C 6 alkylene, substituted or unsubstituted C
  • each R 9 is independently selected from H, substituted or unsubstituted Ci-C 6 alkyl,
  • C 6 fiuoroalkyl a substituted or unsubstituted C 3 -Ciocycloalkyl, a substituted or unsubstituted C 2 -Ci 0 heterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted heteroaryl, -Ci-C 4 alkylene-(substituted or unsubstituted C 3 - Ciocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted C2-Cioheterocycloalkyl), - Ci-C 4 alkylene-(substituted or unsubstituted aryl), and -Ci-C 4 alkylene-(substituted or unsubstituted heteroaryl); or
  • R 10 is substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 heteroalkyl, substituted or unsubstituted Ci-C 6 fiuoroalkyl, a substituted or unsubstituted C 3 - Ciocycloalkyl, a substituted or unsubstituted C 2 -Ci 0 heterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted heteroaryl, -Ci-C 4 alkylene-(substituted or unsubstituted C 3 -Ciocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted C 2 - Cioheterocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted aryl), or -C r
  • R 11 is H or Ci-C 4 alkyl.
  • ring A is selected from pyrrolyl, thiazolyl, oxazolyl, isoxazolyl, oxadiazol l, imidazolyl, pyrazol l, isothiazolyl, triazolyl, and tetrazolyl.
  • X is S. In some embodiments, X is NR A .
  • the compound described herein has the structure of Formula
  • p 0, 1, 2, or 3.
  • Ci-C 6 alkyl substituted or unsubstituted Ci-C 6 fiuoroaikyl, substituted or unsubstituted Ci-C 6 fiuoroalkoxy, substituted or unsubstituted Ci-C 6 alkoxy, substituted or unsubstituted phenyl or substituted or unsubstituted monocyclic heteroaryl.
  • each R 4 is independently selected from H, halogen, -CN, -N0 2 , - OH, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 fiuoroalkyl, substituted or unsubstituted Ci-C 6 fiuoroaikoxy, and substituted or unsubstituted Ci-C 6 alkoxy;
  • R 5 is substituted or unsubstituted C 2 -Ci 0 alkyl, substituted or unsubstituted C 2 -Ci 0 fluoroalkyl, substituted or unsubstituted C 2 -Cioalkoxy, substituted or unsubstituted C 2 -Ciofluoroalkoxy, substituted or unsubstituted C 2 -Ci 0 heteroalkyl, substituted or unsubstituted C 2 - Cioheterofluoroalkyl, or
  • each R 4 is independently selected from H, halogen, -CN, -N0 2 , - OH, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 fiuoroalkyl, substituted or unsubstituted Ci-C 6 fiuoroaikoxy, and substituted or unsubstituted Ci-C 6 alkoxy;
  • each R is independently selected from H, -OH, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 alkoxy, and substituted or unsubstituted Cr
  • R 1 are taken together with the carbon atom to which they are attached to form a substituted or unsubstituted C 3 -Ci 0 cycloalkyl or a substituted or unsubstituted C 2 - Cioheterocycloalkyl;
  • X 1 is CR A or N
  • X 2 is CR A or N
  • X 3 is CR A or N; provided that at least two of X 1 , X 2 , and X 3 is CR A ;
  • ring B is phenyl, naphthyl, monocyclic heteroaryl, or bicyclic heteroaryl;
  • n 0, 1, or 2;
  • L 2 is substituted or unsubstituted Ci-C 6 alkylene, substituted or unsubstituted C
  • each R 9 is independently selected from H, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 heteroalkyl, substituted or unsubstituted Ci- C 6 fluoroalkyl, a substituted or unsubstituted C 3 -Ci 0 cycloalkyl, a substituted or unsubstituted C 2 -Ci 0 heterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted benzyl, a substituted or unsubstituted heteroaryl, -Ci- C 4 alkylene-(substituted or unsubstituted C 3 -Ci 0 cycloalkyl), -CrQalkylene- (substituted or unsubstituted C 2 -Ci 0 heterocycloalkyl), -Ci-C 4 alkylene-(substitute
  • R 10 is substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci- C 6 heteroalkyl, substituted or unsubstituted Ci-C 6 fiuoroaikyl, a substituted or unsubstituted C 3 -Ci 0 cycloalkyl, a substituted or unsubstituted C 2 - Cioheterocycloalkyl, a substituted or unsubstituted aryl, a substituted or
  • 1 1 is H or C C 4 alkyl.
  • the compound of Formula (IV) has the structure of Formula (V):
  • ring B is phenyl
  • R 4 is H, halogen, -CN, -OH, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 fluoroalkyl, substituted or unsubstituted Ci-C 6 fluoroalkoxy, or substituted or unsubstituted Ci-C 6 alkoxy
  • N(R 9 ) 2 substituted or unsubstituted C 2 -Ci 0 alkyl, substituted or unsubstituted C 2 -Ci 0 fluoroalkyl, substituted or unsubstituted Ci-Ci 0 fluoroalkoxy, substituted or unsubstituted Ci-Ci 0 alkoxy, substituted or unsubstituted Ci-Cioheteroalkyl, substituted or unsubstituted C 3 -Ciocycloalkyl, substituted or unsubstituted C 2 -Ci 0 heterocycloalkyl, substituted or unsubstituted phenyl, substituted or unsubstituted monocyclic heteroaryl, or -L'-I ⁇ -R 6 ;
  • Ci-C 6 alkyl substituted or unsubstituted Ci-C 6 fluoroalkyl, substituted or unsubstituted Ci-C 6 fluoroalkoxy, or substituted or unsubstituted Ci-C 6 alkoxy.
  • the compound of Formula (I), (la), (II), (IV) or (V) has the structure of Formula (VI):
  • the compound of Formula (I), (la), (II), (IV) or (V) has the structure of Formula (VI):
  • R A is H, halogen, -OH, C C 6 alkyl, CrC 6 fluoroalkyl, Ci-C 6 fluoroalkoxy, or Ci-C 6 alkoxy;
  • both R 1 are taken together with the carbon atom to which they are attached to form a C3- C 6 cycloalkyl
  • each R 1 is independently Ci-C 4 alkyl
  • R 4 is H, halogen, -OH, C C 4 alkyl, Ci-C 4 fluoroalkyl, Ci-C 4 fluoroalkoxy, or C
  • R 5 is -L'-I ⁇ -R 6 or -L'-R 7 ;
  • L 2 is C C 6 alkylene, C C 6 fluoroalkylene or C C 6 heteroalkylene;
  • R 7 is substituted or unsubstitute
  • R 4 is H, halogen, -CN, -OH, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 fluoroalkyl, substituted or unsubstituted Ci-C 6 fluoroalkoxy, or substituted or unsubstituted Ci-C 6 alkoxy;
  • each R 1 is independently selected from H, -OH, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 alkoxy, and substituted or unsubstituted C C 6 fiuoroalkyl;
  • R 1 are taken together with the carbon atom to which they are attached to form a substituted or unsubstituted C 3 -Ci 0 cycloalkyl or a substituted or unsubstituted C 2 - Cioheterocycloalkyl;
  • Ceheteroalkyl substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted phenyl or substituted or unsubstituted monocyclic heteroaryl;
  • ring B is 5-membered heteroaryl, bicyclic heteroaryl or naphthyl
  • n 0, 1, or 2;
  • R 4 is H, halogen, -CN, -N0 2 , -OH, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 fiuoroalkyl, substituted or unsubstituted Ci-C 6 fiuoroalkoxy, or substituted or unsubstituted Ci-C 6 alkoxy;
  • Cioheteroalkyl substituted or unsubstituted C3-Ciocycloalkyl, substituted or unsubstituted C 2 -Ci 0 heterocycloalkyl, substituted or unsubstituted phenyl, substituted or unsubstituted monocyclic heteroaryl, or -L 1 -L 2 -R 6 ;
  • L 2 is substituted or unsubstituted Ci-C 6 alkylene, substituted or unsubstituted C
  • each R 9 is independently selected from H, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 heteroalkyl, substituted or unsubstituted C C 6 fluoroalkyl, a substituted or unsubstituted C 3 -Ci 0 cycloalkyl, a substituted or unsubstituted C 2 -Cioheterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted benzyl, a substituted or unsubstituted heteroaryl, -Cr C 4 alkylene-(substituted or unsubstituted C 3 -Ci 0 cycloalkyl), -Ci-C 4 alkylene- (substituted or unsubstituted C 2 -Cioheterocycloalkyl), -Ci-C 4 alkylene-(substi
  • R 10 is substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Cr
  • C 6 heteroalkyl substituted or unsubstituted Ci-C 6 fiuoroaikyl, a substituted or unsubstituted C 3 -Ciocycloalkyl, a substituted or unsubstituted C 2 - Cioheterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted benzyl, a substituted or unsubstituted heteroaryl, -Ci-C 4 alkylene- (substituted or unsubstituted C 3 -Ciocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted C 2 -Ci 0 heterocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted aryl), or -Ci-C 4 alkylene-(substituted or unsubstituted hetero
  • R 11 is H or Ci-C 4 alkyl.
  • each R 1 is independently selected from H, -OH, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 alkoxy, and substituted or unsubstituted C
  • R 1 are taken together with the carbon atom to which they are attached to form a substituted or unsubstituted C 3 -C 6 cycloalkyl or a substituted or unsubstituted C 2 - C 6 heterocycloalkyl;
  • X is O or S
  • each R A is independently selected from H, halogen, -CN, -N0 2 , -OH, -OR 9 , -SR 9 , -
  • ring B is phenyl, naphthyl, monocyclic heteroaryl, or bicyclic heteroaryl;
  • n 0, 1, or 2;
  • L 2 is substituted or unsubstituted Ci-C 6 alkylene, substituted or unsubstituted C
  • each R 9 is independently selected from H, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 heteroalkyl, substituted or unsubstituted Ci- C 6 fluoroalkyl, a substituted or unsubstituted C 3 -Ci 0 cycloalkyl, a substituted or unsubstituted C 2 -Cioheterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted benzyl, a substituted or unsubstituted heteroaryl, -Ci- C 4 alkylene-(substituted or unsubstituted C 3 -Ci 0 cycloalkyl), -CrQalkylene- (substituted or unsubstituted C 2 -Cioheterocycloalkyl), -Ci-C 4 alkylene-(substi
  • R 10 is substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci- C 6 heteroalkyl, substituted or unsubstituted Ci-C 6 fiuoroaikyl, a substituted or unsubstituted C 3 -Ciocycloalkyl, a substituted or unsubstituted C 2 - Cioheterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted benzyl, a substituted or unsubstituted heteroaryl, -Ci-C 4 alkylene- (substituted or unsubstituted C 3 -Ciocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted C 2 -Ci 0 heterocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstit
  • R 11 is H or Ci-C 4 alkyl.
  • L 2 is substituted or unsubstituted C C 6 alkylene, substituted or unsubstituted Ci-C 6 fluoroalkylene or substituted or unsubstituted Ci C 6 heteroalkylene;
  • each R A is independently selected from H, halogen, -CN, -N0 2 ,
  • both R 1 are taken together with the carbon atom to which they are attached to form a substituted or unsubstituted C 3 -C 6 cycloalkyl or a substituted or unsubstituted C 2 - C 6 heterocycloalkyl;
  • each R 1 is independently H, -OH, Ci-C 6 alkyl, Ci-C 6 alkoxy, or Ci-C 6 iluoroalkyl;
  • X is O or S
  • R A is C C 6 alkyl
  • ring B is phenyl, naphthyl, monocyclic heteroaryl, or bicyclic heteroaryl;
  • n 0, 1, or 2;
  • L 2 is Ci-C 6 alkylene, Ci-C 6 fluoroalkylene or Ci-C 6 heteroalkylene;
  • each R 9 is independently selected from H, Ci-C 6 alkyl, Ci-C 6 heteroalkyl, Ci-
  • C 6 fluoroalkyl a substituted or unsubstituted C 3 -Ci 0 cycloalkyl, a substituted or unsubstituted C 2 -Cioheterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted benzyl, a substituted or unsubstituted heteroaryl, -Ci- C 4 alkylene-(substituted or unsubstituted C 3 -Ci 0 cycloalkyl), -CrQalkylene- (substituted or unsubstituted C 2 -Cioheterocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted aryl), and -Ci-C 4 alkylene-(substituted or unsubstituted heteroaryl); or two R 9 groups attached to the same N atom are
  • R 10 is Ci-C 6 alkyl, Ci-C 6 heteroalkyl, Ci-C 6 fluoroalkyl, a substituted or unsubstituted C 3 - Ciocycloalkyl, a substituted or unsubstituted C 2 -Ci 0 heterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted benzyl, a substituted or unsubstituted heteroaryl, -Ci-C 4 alkylene-(substituted or unsubstituted C 3 - Ciocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted C 2 - Cioheterocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted aryl), or -Ci- C 4 alkylene-(substituted or unsubstituted
  • R 11 is H or C C 4 alkyl.
  • L 2 is C C 6 alkylene, d-Cefluoroalkylene or C C 6 heteroalkylene;
  • R 6 is -CN, -N0 2
  • R A is Ci-C 6 alkyl; both R 1 are taken together with the carbon atom to which they are attached to form a C3-C 6 cycloalkyl; or each R 1 is independently Cr
  • the compound of Formula (VIII) has the structure of Formula
  • each R A is independently selected from H, halogen, -OH, C C 6 alkyl, and Ci-C 6 alkoxy.
  • the compound of Formula (VIII) or Formula (Villa) has the structure of Formula (IXa):
  • each R 9 is independently selected from H, Ci-C 6 alkyl, Ci- C 6 heteroalkyl, Ci-C 6 fiuoroaikyl, a substituted or unsubstituted C 3 -C 6 cycloalkyl, a substituted or unsubstituted C 2 -C 6 heterocycloalkyl, a substituted or unsubstituted phenyl, a substituted or unsubstituted benzyl, and a substituted or unsubstituted monocyclic heteroaryl; or two R 9 groups attached to the same N atom are taken together with the N atom to which they are attached to form a substituted or unsubstituted C 2 -C 6 heterocycloalkyl; R is Ci-C 6 alkyl, C C 6 heteroalkyl, Ci-C 6 iluoroalkyl, a substituted or unsubstituted C3-C 6 cycloalkyl, a substituted or unsubstituted
  • R A is -CH 3 ; both R 1 are taken together with the carbon atom to which they are attached to form a cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl; or each R 1 is -CH 3 ;
  • L 2 is C C 6 alkylene;
  • R 6 is substituted or unsubstituted C 2 -C 6 heterocycloalkyl, substituted or unsubstituted monocyclic heteroaryl, or substituted or unsubstituted phenyl
  • each R is independently selected from H and -CH 3 ;
  • R 1 are taken together with the carbon atom to which they are attached to form a cyclobutyl
  • X is O or S; X 1 is CH or N;
  • each R 1 is independently selected from H and -CH 3 ;
  • R 1 are taken together with the carbon atom to which they are attached to form cyclobutyl
  • X is O
  • X 1 is CH or N
  • each R 1 is independently selected from H and -CH 3 ;
  • R 1 are taken together with the carbon atom to which they are attached to form cyclobutyl
  • X is O or S
  • X I is CH or N
  • compounds disclosed herein are selective androgen receptor modulators.
  • compounds disclosed herein have high specificity for the androgen receptor and have desirable, tissue-selective pharmacological activities. Desirable, tissue-selective pharmacological activities include, but are not limited to, AR antagonist activity in prostate cells and no AR antagonist activity in non-prostrate cells.
  • compounds disclosed herein are antiandrogens that display negligible or no AR agonist activity.
  • presented herein are compounds selected from active metabolites, tautomers, pharmaceutically acceptable solvates, pharmaceutically acceptable salts or prodrugs of a compound of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X).
  • a pharmaceutical composition comprising a therapeutically effective amount of a compound of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X).
  • the pharmaceutical composition also contains at least one pharmaceutically acceptable inactive ingredient.
  • the pharmaceutical composition is formulated for intravenous injection, subcutaneous injection, oral administration, or topical administration.
  • the pharmaceutical composition is a tablet, a pill, a capsule, a liquid, a suspension, a gel, a colloid, a dispersion, a suspension, a solution, an emulsion, an ointment, or a lotion.
  • the pharmaceutical composition further comprises one or more additional therapeutically active agents selected from: corticosteroids, anti-emetic agents, analgesics, anti-cancer agents, anti-inflammatories, kinase inhibitors, HSP90 inhibitors, histone deacetylase (HDAC) inhibitors.
  • additional therapeutically active agents selected from: corticosteroids, anti-emetic agents, analgesics, anti-cancer agents, anti-inflammatories, kinase inhibitors, HSP90 inhibitors, histone deacetylase (HDAC) inhibitors.
  • a method comprising administering a compound of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X) to a human with a diseases or condition that is androgen receptor meditated or androgen receptor dependent.
  • the human is already being administered one or more additional therapeutically active agents other than a compound of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X).
  • the method further comprises administering one or more additional therapeutically active agents other than a compound of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X).
  • the one or more additional therapeutically active agents other than a compound of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X) are selected from: corticosteroids, anti-emetic agents, analgesics, anti-cancer agents, anti-inflammatories, kinase inhibitors, HSP90 inhibitors, histone deacetylase (HDAC) inhibitors.
  • described herein is a method of treating an androgen receptor dependent or androgen receptor mediated disease or condition in mammal comprising administering to the mammal a therapeutically effective amount of a compound of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X), or a pharmaceutically acceptable salt thereof or N-oxide thereof.
  • the adrogen receptor dependent or androgen receptor mediated disease or condition is benign prostate hyperplasia, hirsutism, acne, adenomas and neoplasies of the prostate, benign or malignant tumor cells containing the androgen receptor, hyperpilosity, seborrhea, endometriosis, polycystic ovary syndrome, androgenic alopecia, hypogonadism, osteoporosis, suppression of spermatogenesis, libido, cachexia, anorexia, androgen supplementation for age related decreased testosterone levels, prostate cancer, breast cancer, endometrial cancer, uterine cancer, hot flashes, and Kennedy's disease muscle atrophy and weakness, skin atrophy, bone loss, anemia,
  • arteriosclerosis cardiovascular disease
  • loss of energy loss of well-being
  • type 2 diabetes type 2 diabetes or abdominal fat accumulation.
  • a method of treating cancer in a mammal comprising administering to the mammal a thereapuetically effective amount of a compound of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X), or a pharmaceutically acceptable salt thereof or N-oxide thereof.
  • the cancer is a hormone dependent cancer.
  • the hormone dependent cancer is an androgen receptor dependent cancer.
  • the cancer is prostate cancer.
  • the cancer is hormone refractory prostate cancer.
  • the method of treating cancer further comprises administering to the mammal at least one additional anti-cancer agent.
  • described herein is a method of treating cancer in a mammal comprising administering to the mammal a thereapuetically effective amount of a compound, wherein the compound is: an androgen receptor inverse agonist; androgen receptor antagonist; androgen receptor degrader; androgen receptor trafficking modulator; androgen receptor degrader; androgen receptor DNA-binding inhibitor; or combinations thereof.
  • the cancer is prostate cancer.
  • the cancer is hormone refractory prostate cancer.
  • the compound is a compound of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X), or a pharmaceutically acceptable salt thereof or N-oxide thereof.
  • Pharmaceutical formulations described herein are administerable to a subject in a variety of ways by multiple administration routes, including but not limited to, oral, parenteral (e.g., intravenous, subcutaneous, intramuscular), buccal, topical or transdermal administration routes.
  • the pharmaceutical formulations described herein include, but are not limited to, aqueous liquid dispersions, self-emulsifying dispersions, solid solutions, liposomal dispersions, solid dosage forms, powders, immediate release formulations, controlled release formulations, fast melt formulations, tablets, capsules, pills, delayed release formulations, extended release formulations, pulsatile release formulations, multiparticulate formulations, and mixed immediate and controlled release formulations.
  • the compounds of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) and (X) are administered orally.
  • the compounds of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) and (X) are administered topically.
  • the compound of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X) is formulated into a variety of topically administrable compositions, such as solutions, suspensions, lotions, gels, pastes, shampoos, scrubs, rubs, smears, medicated sticks, medicated bandages, balms, creams or ointments.
  • Such pharmaceutical compounds can contain solubilizers, stabilizers, tonicity enhancing agents, buffers and preservatives.
  • the compounds of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) and (X) are administered topically to the skin.
  • the disease or condition is any of the diseases or conditions specified herein.
  • any of the aforementioned aspects are further embodiments in which: (a) the effective amount of the compound of Formula (I), (II), (III), (IV), (V), (VI), (VII), (VIII), (IX) or (X) is systemically administered to the mammal; and/or (b) the effective amount of the compound is administered orally to the mammal; and/or (c) the effective amount of the compound is intravenously administered to the mammal; and/or (d) the effective amount of the compound is administered by injection to the mammal; and/or (e) the effective amount of the compound is administered topically to the mammal; and/or (f) the effective amount is adminstered non- systemically or locally to the mammal.
  • any of the aforementioned aspects are further embodiments comprising single administrations of the effective amount of the compound, including further embodiments in which (i) the compound is administered once; (ii) the compound is administered to the mammal multiple times over the span of one day; (iii) continually; or (iv) continuously.
  • any of the aforementioned aspects are further embodiments comprising multiple administrations of the effective amount of the compound, including further embodiments in which (i) the compound is administered continuously or intermittently: as in a a single dose; (ii) the time between multiple administrations is every 6 hours; (iii) the compound is administered to the mammal every 8 hours; (iv) the compound is administered to the mammal every 12 hours; (v) the compound is administered to the mammal every 24 hours.
  • the method comprises a drug holiday, wherein the administration of the compound is temporarily suspended or the dose of the compound being administered is temporarily reduced; at the end of the drug holiday, dosing of the compound is resumed.
  • the length of the drug holiday varies from 2 days to 1 year.
  • a method of reducing AR activation in a mammal comprising administering to the mammal at least one compound having the structure of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X).
  • the method comprises reducing AR activation in prostate cells in the mammal.
  • the method comprises reducing AR activation in prostate cells in the mammal and not in non-prostrate cells.
  • the method of reducing AR activation comprises reducing the binding of androgens to the androgen receptor.
  • the method of reducing AR activation comprises reducing AR concentrations.
  • the disease or condition is prostrate cancer.
  • the androgen receptor dependent or androgen receptor mediated disease or condition is described herein.
  • the mammal is a human.
  • compounds provided herein are administered to a human.
  • compounds provided herein are orally administered.
  • compounds provided herein are used to diminish, reduce, or eliminate the activity of androgen receptors.
  • Articles of manufacture which include packaging material, a compound of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X) within the packaging material, and a label that indicates that the compound or composition, or pharmaceutically acceptable salt, tautomers, pharmaceutically acceptable N-oxide, pharmaceutically active metabolite, pharmaceutically acceptable prodrug, or pharmaceutically acceptable solvate thereof, is used for reducing, diminishing or eliminating the effects of androgen receptors, or for the treatment, prevention or amelioration of one or more symptoms of a disease or condition that would benefit from a reduction or elimination of androgen receptor activity, are provided.
  • Androgen receptor is a member of the steroid and nuclear receptor superfamily. Among this large family of proteins, only five vertebrate steroid receptors are known and include the androgen receptor, estrogen receptor, progesterone receptor, glucocorticoid receptor, and mineralocorticoid receptor. AR is a soluble protein that functions as an intracellular transcriptional factor. AR function is regulated by the binding of androgens, which initiates sequential conformational changes of the receptor that affect receptor-protein interactions and receptor-DNA interactions.
  • AR is mainly expressed in androgen target tissues, such as the prostate, skeletal muscle, liver, and central nervous system (CNS), with the highest expression level observed in the prostate, adrenal gland, and epididymis. AR can be activated by the binding of endogenous androgens, including testosterone and 5a-dihydrotestosterone (5a-DHT).
  • androgen target tissues such as the prostate, skeletal muscle, liver, and central nervous system (CNS)
  • CNS central nervous system
  • AR can be activated by the binding of endogenous androgens, including testosterone and 5a-dihydrotestosterone (5a-DHT).
  • the androgen receptor (AR) located on Xql 1-12 is a 110 kD nuclear receptor that, upon activation by androgens, mediates transcription of target genes that modulate growth and differentiation of prostate epithelial cells. Similar to the other steroid receptors, unbound AR is mainly located in the cytoplasm and associated with a complex of heat shock proteins (HSPs) through interactions with the ligand-binding domain. Upon agonist binding, AR goes through a series of conformational changes: the heat shock proteins dissociate from AR, and the transformed AR undergoes dimerization, phosphorylation, and translocation to the nucleus, which is mediated by the nuclear localization signal.
  • HSPs heat shock proteins
  • Translocated receptor then binds to the androgen response element (ARE), which is characterized by the six-nucleotide half-site consensus sequence 5'-TGTTCT-3' spaced by three random nucleotides and is located in the promoter or enhancer region of AR gene targets.
  • ARE androgen response element
  • Recruitment of other transcription co- regulators (including co-activators and co-repressors) and transcriptional machinery further ensures the transactivation of AR-regulated gene expression. All of these processes are initiated by the ligand-induced conformational changes in the ligand-binding domain.
  • AR signaling is crucial for the development and maintenance of male reproductive organs including the prostate gland, as genetic males harboring loss of function AR mutations and mice engineered with AR defects do not develop prostates or prostate cancer. This dependence of prostate cells on AR signaling continues even upon neoplastic transformation. Androgen depletion (now using GnRH agonists) continues to be the mainstay of prostate cancer treatment. However androgen depletion is usually effective for a limited duration and prostate cancer evolves to regain the ability to grow despite low levels of circulating androgens.
  • CRPC castration resistant prostate cancer
  • Prostate cancer is the second most common cause of cancer death in men in the US, and approximately one in every six American men will be diagnosed with the disease during his lifetime. Treatment aimed at eradicating the tumor is unsuccessful in 30% of men, who develop recurrent disease that is usually manifest first as a rise in plasma prostate-specific antigen (PSA) followed by spread to distant sites.
  • PSA prostate-specific antigen
  • AR androgen receptor
  • these men are treated with agents that block production of testosterone (e.g. GnRH agonists), alone or in combination with anti-androgens (e.g.
  • bicalutamide which antagonize the effect of any residual testosterone.
  • the approach is effective as evidenced by a drop in PSA and regression of visible tumor (if present); however, this is followed by regrowth as a "castration resistant" prostate cancer (CRPC) to which most patients eventually succumb.
  • CRPC castration resistant prostate cancer
  • Recent studies on the molecular basis of CRPC have demonstrated that CRPC continues to depend on AR signaling and that a key mechanism of acquired resistance is an elevated level of AR protein (Nat. Med, 2004, 10, 33-39).
  • AR targeting agents with activity in hormone sensitive and castration resistant resistant prostate cancer have great promise in treating this lethal disease.
  • Anti-androgens are useful for the treatment of prostate cancer during its early stages.
  • prostate cancer often advances to a hormone-refractory state in which the disease progresses in the presence of continued androgen ablation or anti-androgen therapy.
  • Instances of antiandrogen withdrawal syndrome have also been reported after prolonged treatment with anti-androgens.
  • Antiandrogen withdrawal syndrome is commonly observed clinically and is defined in terms of the tumor regression or symptomatic relief observed upon cessation of antiandrogen therapy.
  • AR mutations that result in receptor promiscuity and the ability of these anti-androgens to exhibit agonist activity might at least partially account for this phenomenon. For example, hydroxyflutamide and bicalutamide act as AR agonists in T877A and
  • compounds disclosed herein are useful in the treatment of prostrate cancer, either alone or in combination with other agent agents that can modulate other critical pathways in prostate cancer, including but not limited to those that target IGF1R, the PDK/AKT/mTOR axis, HSP90, or histone deacetylases.
  • AR-related diseases or conditions include, but are not limited to, benign prostate hyperplasia, hirsutism, acne, adenomas and neoplasies of the prostate, benign or malignant tumor cells containing the androgen receptor, hyperpilosity, seborrhea, endometriosis, polycystic ovary syndrome, androgenic alopecia, hypogonadism, osteoporosis, suppression of spermatogenesis, libido, cachexia, anorexia, androgen supplementation for age related decreased testosterone levels, prostate cancer, breast cancer, endometrial cancer, uterine cancer, hot flashes, and Kennedy's disease muscle atrophy and weakness, skin atrophy, bone loss, anemia, arteriosclerosis, cardiovascular disease, loss of energy, loss of well-being, type 2 diabetes and abdominal fat accumulation.
  • compounds disclosed herein inhibit AR nuclear translocation, DNA binding to androgen response elements, and coactivator recruitment.
  • compounds disclosed herein inhibit AR nuclear translocation, DNA binding to androgen response elements, and coactivator recruitment.
  • compounds disclosed herein exhibit no agonist activity in AR-overexpressing prostate cancer cells.
  • compounds disclosed herein are used to treat prostrate cancer in a mammal, wherein the mammal is chemotherapy-nai ' ve.
  • compounds disclosed herein are used to treat prostrate cancer in a mammal, wherein the mammal is being treated for prostrate cancer with at least one anticancer agent.
  • the prostrate cancer is hormone refractory prostate cancer.
  • the prostrate cancer is bicalutamide-resistant prostate cancer.
  • Compounds of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) and (X), including pharmaceutically acceptable salts, prodrugs, and pharmaceutically acceptable solvates thereof, are androgen receptor modulators, such as, for example, AR inverse agonists, AR antagonists, AR degraders, AR trafficking modulators and/or AR DNA-binding inhibitors, and are useful in the treatment of androgen receptor-dependent or androgen receptor -mediated conditions or diseases of diseases or conditions.
  • ring A is monocyclic heteroaryl, bicyclic heteroaryl, or naphthyl
  • n 0, 1, 2, 3 or 4;
  • each R A is independently selected from H, halogen, -CN, -N0 2 , -OH, -OR 9 , -SR 9 , -
  • each R 1 is independently selected from H, -OH, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 alkoxy, and substituted or unsubstituted C
  • R 1 are taken together with the carbon atom to which they are attached to form a substituted or unsubstituted C3-Ciocycloalkyl or a substituted or unsubstituted C 2 - Cioheterocycloalkyl;
  • ring B is phenyl, naphthyl, monocyclic heteroaryl, or bicyclic heteroaryl;
  • n 0, 1, 2, 3 or 4;
  • each R 4 is independently selected from H, halogen, -CN, -N0 2 , -OH, -OR 9 , -SR 9 , -
  • R 5 is substituted or unsubstituted C 2 -Cioalkyl, substituted or unsubstituted C 2 -
  • Ciofluoroalkyl substituted or unsubstituted C 2 -Ci 0 alkoxy, substituted or unsubstituted C 2 -Ciofluoroalkoxy, substituted or unsubstituted C 2 -Cioheteroalkyl, substituted or unsubstituted C 2 -Cioheterofluoroalkyl, or -L'- ⁇ -R 6 ;
  • L 2 is substituted or unsubstituted Ci-C 6 alkylene, substituted or unsubstituted C
  • R 10 is substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 heteroalkyl, substituted or unsubstituted Ci-C 6 fiuoroaikyl, a substituted or unsubstituted C 3 - Ciocycloalkyl, a substituted or unsubstituted C 2 -Ci 0 heterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted benzyl, a substituted or unsubstituted heteroaryl, -Ci-C 4 alkylene-(substituted or unsubstituted C 3 -Ci 0 cycloalkyl), -C
  • R 11 is H or Ci-C 4 alkyl.
  • substituents are selected from among from a subset of the listed alternatives.
  • both R 1 are taken together with the carbon atom to which they are attached to form a substituted or unsubstituted C 3 - Ciocycloalkyl.
  • both R 1 are taken together with the carbon atom to which they are attached to form a C 3 -C 6 Cycloalkyl.
  • both R 1 are taken together with the carbon atom to which they are attached to form a substituted or unsubstituted cyclopropyl, cyclobutyl, cyclopentyl, or cyclcohexyl.
  • both R 1 are taken together with the carbon atom to which they are attached to form a cyclopropyl. In some embodiments, both R 1 are taken together with the carbon atom to which they are attached to form a cyclobutyl. In some embodiments, both R 1 are taken together with the carbon atom to which they are attached to form a cyclopentyl. In some embodiments, both R 1 are taken together with the carbon atom to which they are attached to form a cyclohexyl. In some embodiments, each R 1 is independently selected from H, -OH, Ci-C 6 alkyl, and Ci-C 6 fluoroalkyl. In some embodiments, each R 1 is independently selected from H, -CH 3 and -CF 3 .
  • ring A is C-linked monocyclic heteroaryl, C-linked bicyclic heteroaryl, or naphthyl. In some embodiments, ring A is C-linked monocyclic heteroaryl. In some embodiments, ring A is C-linked monocyclic 5-membered or 6-membered heteroaryl. In some embodiments, ring A is C-linked monocyclic 6-membered heteroaryl. In some embodiments, ring A is an N-containing heteroaryl.
  • both R 1 are taken together with the carbon atom to which they are attached to form a cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl;
  • ring A is N- containing monocyclic heteroaryl selected from pyridinyl, pyrimidinyl, pyridazinyl, pyrazinyl, triazinyl, pyrrolyl, thiazolyl, oxazolyl, isoxazolyl, oxadiazolyl, imidazolyl, pyrazolyl, isothiazolyl, triazolyl, and tetrazolyl.
  • ring A is pyridinyl, pyrimidinyl, pyridazinyl, or pyrazinyl. In some embodiments, ring A is pyridinyl. 124] In some embodiments, . In some embodiments,
  • ring A is monosubstituted with R A . In some embodiments, ring A is disubstituted with R A . In some embodiments, ring A is trisubstituted with R A . In some embodiments, ring A is substituted with -CN and at least one additional R A . In some embodiments, ring A is substituted with -CN and zero, one or two additional R A . In some embodiments, ring A is substituted with -CN and one or two additional R A . In some embodiments, ring A is substituted with -CN and one additional R A . In some embodiments, ring A is substituted with -CN and one additional R A .
  • both R 1 are taken together with the carbon atom to which they are attached to form a cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl;
  • ring A is N- containing bicyclic heteroaryl selected from quinolinyl, isoquinolinyl, quinazolinyl, quinoxalinyl, naphthyridinyl, indolyl, indazolyl, benzoxazolyl, benzisoxazolyl, benzofuranyl, benzothienyl, benzothiazolyl, benzimidazolyl, purinyl, cinnolinyl, phthalazinyl, pteridinyl, pyridopyrimidinyl, pyrazolopyrimidinyl, azaindolyl, pyrazolopyridinyl, thiazolopyrimidinyl, triazolopyridazin
  • ring A is N-containing bicyclic heteroaryl selected from quinolinyl, isoquinolinyl, quinazolinyl, quinoxalinyl, pyridopyrimidinyl, pyrazolopyrimidinyl, triazolopyridazinyl, and pyrrolopyrimidinyl.
  • ring A is [l,2,4]triazolo[4,3-b]pyridazinyl.
  • ring B is phenyl or monocyclic heteroaryl; each R 4 is independently selected from H, halogen, -CN, -N0 2 , -OH, substituted or unsubstituted C C 6 alkyl, substituted or unsubstituted Ci-C 6 fiuoroalkyl, substituted or unsubstituted C
  • R 5 is substituted or unsubstituted C 2 -Ci 0 alkyl, substituted or unsubstituted C 2 - Ciofluoroalkyl, substituted or unsubstituted C 2 -Ci 0 alkoxy, substituted or unsubstituted C 2 -
  • Ciofluoroalkoxy substituted or unsubstituted C 2 -Cioheteroalkyl, substituted or unsubstituted C 2 - doheterofluoroalkyl, or -L L -L 2 -R 6 ;
  • L 2 is substituted or unsubstituted C C 6 alkylene, substituted or unsubstituted Ci-C 6 fiuoroalkylene or substituted or unsubstituted Ci- C 6 heteroalkylene;
  • R 6 is halogen, -CN, -N0 2 , -OH, -OR 9
  • ring B is phenyl or monocyclic heteroaryl; each R 4 is independently selected from H, halogen, -CN, -N0 2 , -OH, substituted or unsubstituted C C 4 alkyl, substituted or unsubstituted Ci-C 4 fluoroalkyl, substituted or unsubstituted Cr
  • R 5 is substituted or unsubstituted C 2 -Ci 0 alkyl, substituted or unsubstituted C 2 -Ci 0 fluoroalkyl, substituted or unsubstituted C 2 - Cioalkoxy, substituted or unsubstituted C 2 -Ciofiuoroalkoxy, substituted or unsubstituted C 2 -
  • Cioheteroalkyl substituted or unsubstituted C 2 -Ci 0 heterofluoroalkyl, or -L 1 -L 2 -R 6 ;
  • L 2 is substituted or unsubstituted Ci-C 6 alkylene, substituted or
  • Cioheterocycloalkyl substituted or unsubstituted monocyclic heteroaryl, substituted or unsubstituted bicyclic heteroaryl, substituted or unsubstituted phenyl, or substituted or unsubstituted naphthyl.
  • L 2 is substituted or unsubstituted Ci-C 6 alkylene;
  • R 6 is substituted or unsubstituted C 3 -Ci 0 cycloalkyl, substituted or unsubstituted C2-Cioheterocycloalkyl, substituted or unsubstituted monocyclic heteroaryl, substituted or unsubstituted bicyclic heteroaryl, substituted or unsubstituted phenyl, or substituted or unsubstituted naphthyl.
  • L 2 is substituted or unsubstituted Ci-C 6 alkylene;
  • each R 9 is independently selected from H, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted C
  • C 6 fluoroalkyl -Ci-C4alkylene-(substituted or unsubstituted C3-Ciocycloalkyl), -Ci-C 4 alkylene- (substituted or unsubstituted C 2 -Ci 0 heterocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted aryl), and -Ci-C 4 alkylene-(substituted or unsubstituted heteroaryl); or two R 9 groups attached to the same N atom are taken together with the N atom to which they are attached to form a substituted or unsubstituted C 2 -Ci 0 heterocycloalkyl; R 10 is substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 fiuoroalkyl, -Ci-C 4 alkylene- (substituted or unsub
  • ring A is monocyclic heteroaryl, bicyclic heteroaryl, or naphthyl
  • n 1, 2, 3 or 4;
  • each R 1 is independently selected from H, -OH, Ci-C 6 alkyl, Ci-C 6 alkoxy, and C
  • X is S or O
  • ring B is phenyl, naphthyl, monocyclic heteroaryl, or bicyclic heteroaryl;
  • n 0, 1, 2, 3 or 4;
  • R 5 is - ⁇ ⁇ ⁇ -L'-R 7 ;
  • L 2 is Ci-C 6 alkylene, Ci-C 6 fluoroalkylene or Ci-C 6 heteroalkylene;
  • Ci-C 6 fluoroalkyl Ci-C 6 heteroalkyl, substituted or unsubstituted C 3 - Ciocycloalkyl, substituted or unsubstituted C 2 -Ci 0 heterocycloalkyl, substituted or unsubstituted monocyclic heteroaryl, substituted or unsubstituted bicyclic heteroaryl, substituted or unsubstituted phenyl, or substituted or unsubstituted naphthyl;
  • R 7 is substituted or unsubstituted monocyclic C 2 -C 6 heterocycloalkyl, or substituted or unsubstituted monocyclic heteroaryl;
  • each R 9 is independently selected from H, Ci-C 6 alkyl, Ci-C 6 heteroalkyl, Ci-C 6 fiuoroaikyl, substituted or unsubstituted C3-C 6 cycloalkyl, substituted or unsubstituted C 2 -
  • Cioheterocycloalkyl substituted or unsubstituted phenyl, substituted or unsubstituted monocyclic heteroaryl, -Ci-C4alkylene-(substituted or unsubstituted C 3 -C 6 cycloalkyl), - Ci-C4alkylene-(substituted or unsubstituted monocyclic C 2 -C 6 heterocycloalkyl), -Cr C 4 alkylene-(substituted or unsubstituted phenyl), and -Ci-C 4 alkylene-(substituted or unsubstituted monocyclic heteroaryl); or two R 9 groups attached to the same N atom are taken together with the N atom to which they are attached to form a substituted or unsubstituted monocyclic C 2 - C 6 heterocycloalkyl;
  • R 10 is Ci-C 6 alkyl, Ci-C 6 heteroalkyl, Ci-C 6 fluoroalkyl, a substituted or unsubstituted C 3 - C 6 cycloalkyl, a substituted or unsubstituted monocyclic C2-C 6 heterocycloalkyl, a substituted or unsubstituted phenyl, a substituted or unsubstituted benzyl, a substituted or unsubstituted monocyclic heteroaryl, -Ci-C 4 alkylene-(substituted or unsubstituted C 3 - C 6 cycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted monocyclic C 2 - C 6 heterocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted phenyl), or -C C 4 alkylene-(substituted or un
  • R 11 is H or Ci-C 4 alkyl.
  • both R 1 are taken together with the carbon atom to which they are attached to form a substituted or unsubstituted C 3 -C 6 cycloalkyl;
  • X is S;
  • ring B is phenyl or monocyclic heteroaryl.
  • both R 1 are taken together with the carbon atom to which they are attached to form a cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl; ring A is pyridinyl, pyrimidinyl, pyridazinyl, or pyrazinyl.
  • ring B is phenyl;
  • R 5 is -L'-lAR 6 ;
  • L 2 is C C 6 alkylene, Ci-C 6 fluoroalkylene or C C 6 heteroalkylene;
  • L 2 is C C 6 alkylene
  • R 6 is substituted or unsubstituted C3-C 6 cycloalkyl, substituted or unsubstituted C 2 -C 6 heterocycloalkyl, substituted or unsubstituted monocyclic heteroaryl, or substituted or unsubstituted phenyl.
  • L 2 is Ci-C 6 alkylene; R 6 is a substituted or unsubstituted C 2 - C 6 heterocycloalkyl.
  • R 6 is a substituted or unsubstituted C 2 -C 6 heterocycloalkyl.
  • R 6 is a substituted or unsubstituted C 3 - C 6 heterocycloalkyl.
  • R 6 is a substituted or unsubstituted N-containing C 2 - C 6 heterocycloalkyl.
  • ring B is phenyl; each R 4 is independently selected from H, halogen, -CN, -N0 2 , -OH, C C 4 alkyl, Ci-C 4 fluoroalkyl, Ci-C 4 fluoroalkoxy, and C C 4 alkoxy;
  • R 5 is -L'-R 7 ;
  • L 2 is Ci-C6alkylene. In some embodiments, L 2 is Ci-C 4 alkylene. In some embodiments, L 2 is -CH 2 -, -CH 2 CH 2 -, -CH 2 CH 2 CH 2 -, -CH 2 CH 2 CH 2 CH 2 -, - CH 2 CH 2 CH 2 CH 2 -, or -CH 2 CH 2 CH 2 CH 2 CH 2 -. In some embodiments, L 2 is -CH 2 -, - CH 2 CH 2 -, -CH 2 CH 2 CH 2 -, or -CH 2 CH 2 CH 2 CH 2 -.
  • each R 4 is independently selected from H, halogen, -OH, C C 4 alkyl, Ci-C 4 fluoroalkyl, Ci-C 4 fluoroalkoxy, and Ci-C 4 alkoxy.
  • R 5 is -L'-R 7 .
  • R 5 is -L'-R 7 ;
  • R 7 is substituted or unsubstituted monocyclic C 2 - C6heterocycloalkyl, or substituted or unsubstituted monocyclic heteroaryl.
  • R 5 is -L'-R 7 ;
  • R 7 is substituted or unsubstituted monocyclic heteroaryl.
  • the compound of Formula (I) or Formula (la) has the structure of Formula (II):
  • the com ound of Formula (la) has the structure of Formula (II):
  • n 2;
  • R A is H, halogen, -OH, C C 6 alkyl, C C 6 fiuoroalkyl, C i -C 6 fluoroalkoxy, or C i -C 6 alkoxy;
  • n 0 or 1 ;
  • each R 4 is independently selected from H, halogen, -CN, -N0 2 , -OH, Ci-C 6 alkyl, C
  • R 5 is -L'-LAR 6 or -L'-R 7 ;
  • L 2 is Ci-C6alkylene, Ci-C6fluoroalkylene or Ci-C6heteroalkylene;
  • R 7 is substituted or unsubstituted monocyclic C 2 -C 6 heterocycloalkyl, or substituted or unsubstituted monoc tract heteroaryl.
  • R 4 is independently selected from H, halogen, -OH, Ci-C 4 alkyl, Ci-C 4 fluoroalkyl, Ci-C 4 fluoroalkoxy, or C C 4 alkoxy; each R 4 is independently selected from H, halogen, -OH, Ci-C 4 alkyl, Ci-C 4 fluoroalkyl, Ci-C 4 fluoroalkoxy, and Ci-C 4 alkoxy;
  • R 5 is -L l -L 2 -R 6 or -L'-R 7 ;
  • L 2 is C C 6 alkylene, Ci-C 6 fluoroalkylene or C C 6 heteroalkylene;
  • ring A is bicyclic heteroaryl, or naphthyl
  • n 0, 1, 2, or 3;
  • each R A is independently selected from H, halogen, -CN, -N0 2 , -OH, -OR 9 , -SR 9 , -
  • each R 1 is independently selected from H, -OH, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 alkoxy, and substituted or unsubstituted C
  • R 1 are taken together with the carbon atom to which they are attached to form a substituted or unsubstituted C 3 -Ci 0 cycloalkyl or a substituted or unsubstituted C 2 -
  • ring B is phenyl, naphthyl, monocyclic heteroaryl, or bicyclic heteroaryl;
  • L 2 is substituted or unsubstituted Ci-C 6 alkylene, substituted or unsubstituted C
  • each R 9 is independently selected from H, substituted or unsubstituted Ci-C 6 alkyl,
  • C 6 fluoroalkyl a substituted or unsubstituted C 3 -Ci 0 cycloalkyl, a substituted or unsubstituted C 2 -Cioheterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted heteroaryl, -Ci-C 4 alkylene-(substituted or unsubstituted C 3 - Ciocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted C 2 -Ci 0 heterocycloalkyl), - Ci-C 4 alkylene-(substituted or unsubstituted aryl), and -Ci-C 4 alkylene-(substituted or unsubstituted heteroaryl); or two R 9 groups attached to the same N atom are taken together with the N atom to which they are attached to form a substituted or
  • R 10 is substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 heteroalkyl, substituted or unsubstituted Ci-C 6 fiuoroaikyl, a substituted or unsubstituted C 3 - Ciocycloalkyl, a substituted or unsubstituted C2-Cioheterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted heteroaryl, -Ci-C 4 alkylene-(substituted or unsubstituted C 3 -Ci 0 cycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted C 2 - Cioheterocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted aryl), or -Ci- C 4 alky
  • R 11 is H or C C 4 alkyl.
  • ring A is selected from quinolinyl, isoquinolinyl, quinazolinyl, quinoxalinyl, naphthyridinyl, indolyl, indazolyl, benzoxazolyl, benzisoxazolyl, benzofuranyl, benzothienyl, benzothiazolyl, benzimidazolyl, purinyl, cinnolinyl, phthalazinyl, pteridinyl, pyridopyrimidinyl, pyrazolopyrimidinyl, azaindolyl, pyrazolopyridinyl, thiazolopyrimidinyl, triazolopyridazinyl, thiazolopyridinyl, pyridothienyl, pyrimidiothienyl, pyrrolopyrimidinyl and naphthyl.
  • ring A is selected from quinolinyl, isoquinolinyl, quinazolinyl, quinoxalinyl, pyridopyrimidinyl, pyrazolopyrimidinyl, triazolopyridazinyl, pyrrolopyrimidinyl, and napthyl.
  • ring A is [l,2,4]triazolo[4,3-b]pyridazinyl.
  • ring A is a 5-membered heteroaryl
  • n 0, 1, 2, or 3;
  • each R A is independently selected from H, halogen, -CN, -N0 2 , -OH, -OR 9 , -SR 9 , -
  • each R 1 is independently selected from H, -OH, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 alkoxy, and substituted or unsubstituted Ci- C 6 fluoroalkyl;
  • R 1 are taken together with the carbon atom to which they are attached to form a substituted or unsubstituted C3-Ciocycloalkyl or a substituted or unsubstituted C 2 - Cioheterocycloalkyl;
  • ring B is phenyl, naphthyl, monocyclic heteroaryl, or bicyclic heteroaryl;
  • n 0, 1, or 2;
  • each R 4 is independently selected from H, halogen, -CN, -N0 2 , -OH, -OR 9 , -SR 9 , -
  • L 2 is substituted or unsubstituted Ci-C 6 alkylene, substituted or unsubstituted C
  • each R 9 is independently selected from H, substituted or unsubstituted Ci-C 6 alkyl,
  • C 6 fluoroalkyl a substituted or unsubstituted C 3 -Ci 0 cycloalkyl, a substituted or unsubstituted C2-Cioheterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted heteroaryl, -Ci-C 4 alkylene-(substituted or unsubstituted C 3 - Ciocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted C 2 -Ci 0 heterocycloalkyl), - Ci-C 4 alkylene-(substituted or unsubstituted aryl), and -Ci-C 4 alkylene-(substituted or unsubstituted heteroaryl); or
  • R 10 is substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 heteroalkyl, substituted or unsubstituted Ci-C 6 fiuoroalkyl, a substituted or unsubstituted C 3 - Ciocycloalkyl, a substituted or unsubstituted C2-Cioheterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted heteroaryl, -Ci-C 4 alkylene-(substituted or unsubstituted C3-Ciocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted C 2 - Cioheterocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted aryl), or -Ci- C 4 alkylene-(sub
  • R 11 is H or Ci-C 4 alkyl.
  • ring A is selected from pyrrolyl, thiazolyl, oxazolyl, isoxazolyl, oxadiazolyl, imidazolyl, pyrazol l, isothiazolyl, triazolyl, and tetrazolyl.
  • the compound described herein has the structure of Formula (III):
  • p 0, 1, 2, or 3.
  • Ci-C 6 alkyl substituted or unsubstituted Ci-C 6 fiuoroalkyl, substituted or unsubstituted Ci-C 6 fiuoroalkoxy, substituted or unsubstituted Ci-C 6 alkoxy, substituted or unsubstituted phenyl or substituted or unsubstituted monocyclic heteroaryl.
  • each R 4 is independently selected from H, halogen, -CN, -N0 2 , - OH, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 fiuoroalkyl, substituted or unsubstituted Ci-C 6 fiuoroaikoxy, and substituted or unsubstituted Ci-C 6 alkoxy;
  • R 5 is substituted or unsubstituted C 2 -Cioalkyl, substituted or unsubstituted C 2 -Ciofluoroalkyl, substituted or unsubstituted C 2 -Ci 0 alkoxy, substituted or unsubstituted C 2 -Ci 0 fluoroalkoxy, substituted or unsubstituted C 2 -Ci 0 heteroalkyl, substituted or unsubstituted C 2 - Cioheterofluoroalkyl, or
  • each R 4 is independently selected from H, halogen, -CN, -N0 2 , - OH, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 fluoroalkyl, substituted or unsubstituted Ci-C 6 fluoroalkoxy, and substituted or unsubstituted Ci-C 6 alkoxy;
  • the compound described herein has the structure of Formula (III):
  • ring A is monocyclic heteroaryl, bicyclic heteroaryl, or naphthyl
  • n 1 or 2;
  • n 0, 1 or 2;
  • each R 4 is independently selected from H, halogen, -CN, -N0 2 , -OH, -OR 9 , -SR 9 , -
  • R 5 is substituted or unsubstituted C3-Ciocycloalkyl, substituted or unsubstituted C 2 -
  • Cioheterocycloalkyl substituted or unsubstituted phenyl, substituted or unsubstituted monocyclic heteroaryl, -L'-I ⁇ -R 6 or -L'-R 7 ;
  • L 2 is Ci-C 6 alkylene, Ci-C 6 fluoroalkylene or Ci-C 6 heteroalkylene;
  • Ci-C 6 fluoroalkyl Ci-C 6 heteroalkyl, substituted or unsubstituted C 3 - Ciocycloalkyl, substituted or unsubstituted C 2 -Cioheterocycloalkyl, substituted or unsubstituted monocyclic heteroaryl, substituted or unsubstituted bicyclic heteroaryl, substituted or unsubstituted phenyl, or substituted or unsubstituted naphthyl;
  • R 7 is substituted or unsubstituted C 3 -Ci 0 cycloalkyl, substituted or unsubstituted
  • each R 9 is independently selected from H, Ci-C 6 alkyl, Ci-C 6 heteroalkyl, C
  • C 6 fluoroalkyl a substituted or unsubstituted C 3 -Ci 0 cycloalkyl, a substituted or unsubstituted C 2 -Cioheterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted benzyl, a substituted or unsubstituted heteroaryl, -C C 4 alkylene-(substituted or unsubstituted C 3 -Ci 0 cycloalkyl), -CrQalkylene- (substituted or unsubstituted C 2 -Cioheterocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted aryl), and -Ci-C 4 alkylene-(substituted or unsubstituted heteroaryl); or two R 9 groups attached to the same N atom are taken together
  • R 10 is Ci-C 6 alkyl, Ci-C 6 heteroalkyl, Ci-C 6 fluoroalkyl, a substituted or unsubstituted C 3 - Ciocycloalkyl, a substituted or unsubstituted C 2 -Cioheterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted benzyl, a substituted or unsubstituted heteroaryl, -Ci-C4alkylene-(substituted or unsubstituted C 3 - Ciocycloalkyl), -Ci-C4alkylene-(substituted or unsubstituted C 2 - Cioheterocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted aryl), or -C r C 4 alkylene-(substituted or unsubstitute
  • R 11 is H or C C 4 alkyl
  • p 0, 1, 2, or 3.
  • R 5 is C 3 -C 6 cycloalkyl, substituted or unsubstituted C2- C 6 heterocycloalkyl, substituted or unsubstituted phenyl, substituted or unsubstituted monocyclic 5-membered or 6-membered heteroaryl, -L'-I ⁇ -R 6 or -L'-R 7 ;
  • L 2 is Ci-C 6 alkylene;
  • R 6 is C 3 -C 6 cycloalkyl, substituted or unsubstituted C2-C 6 heterocycloalkyl, substituted or unsubstituted monocyclic 5-membered or 6-membered heteroaryl, or substituted or unsubstituted phenyl;
  • R 7 is C 3 -C 6 cycloalkyl, substituted or unsubstituted monocyclic C 2 - C 6 heterocycloalkyl, substituted or
  • each R is independently selected from H, -OH, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 alkoxy, and substituted or unsubstituted Ci- C 6 fluoroalkyl;
  • R 1 are taken together with the carbon atom to which they are attached to form a substituted or unsubstituted C 3 -Ciocycloalkyl or a substituted or unsubstituted C2- Cioheterocycloalkyl;
  • X 1 is CR A or N
  • X 2 is CR A or N
  • X 3 is CR A or N; provided that at least two of X 1 , X 2 , and X 3 is CR A ;
  • each R A is independently selected from H, halogen, -CN, -N0 2 , -OH, -OR 9 , -SR 9 , -
  • ring B is phenyl, naphthyl, monocyclic heteroaryl, or bicyclic heteroaryl;
  • n 0, 1, or 2;
  • L 2 is substituted or unsubstituted Ci-C 6 alkylene, substituted or unsubstituted C
  • each R 9 is independently selected from H, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 heteroalkyl, substituted or unsubstituted C C 6 fluoroalkyl, a substituted or unsubstituted C 3 -Ci 0 cycloalkyl, a substituted or unsubstituted C2-Cioheterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted benzyl, a substituted or unsubstituted heteroaryl, -Ci- C 4 alkylene-(substituted or unsubstituted C 3 -Ci 0 cycloalkyl), -Ci-C 4 alkylene- (substituted or unsubstituted C2-Cioheterocycloalkyl), -Ci-C 4 alkylene-(substituted
  • R 10 is substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted C
  • C 6 heteroalkyl substituted or unsubstituted Ci-C 6 fluoroalkyl, a substituted or unsubstituted C3-Ciocycloalkyl, a substituted or unsubstituted C 2 - Cioheterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted benzyl, a substituted or unsubstituted heteroaryl, -Ci-C 4 alkylene- (substituted or unsubstituted C3-Ciocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted C 2 -Ci 0 heterocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted aryl), or -Ci-C 4 alkylene-(substituted or unsubstituted heteroaryl);
  • R is H or Ci-C 4 alkyl.
  • X 1 is CR A or N
  • X 2 is CR A or N
  • v3 ⁇ ⁇ T A Random_ ni i vl v2 v3 ⁇ /- ⁇ >
  • the com ound of Formula (IV) has the structure of Formula (V):
  • ring B is phenyl
  • R 4 is H, halogen, -CN, -OH, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 fiuoroalkyl, substituted or unsubstituted Ci-C 6 fiuoroalkoxy, or substituted or unsubstituted Ci-C 6 alkoxy
  • N(R 9 ) 2 substituted or unsubstituted C 2 -Cioalkyl, substituted or unsubstituted C 2 -Ciofluoroalkyl, substituted or unsubstituted Ci-Ci 0 fluoroalkoxy, substituted or unsubstituted Ci-Ci 0 alkoxy, substituted or unsubstituted Ci-Ci 0 heteroalkyl, substituted or unsubstituted C 3 -Ci 0 cycloalkyl, substituted or unsubstituted C 2 -Cioheterocycloalkyl, substituted or unsubstituted phenyl, substituted or unsubstituted monocyclic heteroaryl, or -L'-I ⁇ -R 6 ;
  • the compound of Formula (I), (la), (II), (IV) or (V) has the structure of Formula (VI):
  • the compound of Formula (I), (la), (II), (IV) or (V) has the structure of Formula (VI):
  • R A is H, halogen, -OH, C C 6 alkyl, C C 6 fiuoroalkyl, Ci-C 6 fiuoroaikoxy, or Ci-C 6 alkoxy;
  • both R 1 are taken together with the carbon atom to which they are attached to form a C3- C 6 cycloalkyl
  • each R 1 is independently Ci-C 4 alkyl
  • R 4 is H, halogen, -OH, Ci-C 4 alkyl, Ci-C 4 fluoroalkyl, Ci-C 4 fluoroalkoxy, or Ci- C 4 alkoxy.
  • R 5 is -L'-I ⁇ -R 6 or -L'-R 7 ;
  • L 2 is Ci-C 6 alkylene, Ci-C 6 fluoroalkylene or Ci-C 6 heteroalkylene;
  • R 7 is substituted
  • one R A is -CN; and the other R A is H, F, CI, -OH, -CH 3 , -CF 3 , - OCF 3 , -OCH 3 or -OCH 2 CH 3 .
  • one R A is -CN; and the other R A is -CH 3 , or -CF 3 .
  • both R 1 are taken together with the carbon atom to which they are attached to form a cyclobutyl; or each R 1 is -CH 3 .
  • R 5 is -L'-I ⁇ -R 6 or -L'-R 7 ;
  • L 2 is Ci-C 6 alkylene;
  • R 6 is substituted or unsubstituted C 3 -C 6 cycloalkyl, substituted or unsubstituted monocyclic C 2 -C 6 heterocycloalkyl, substituted or unsubstituted monocyclic heteroaryl, or substituted or unsubstituted phenyl;
  • R 7 is substituted or unsubstituted monocyclic C 2 - C 6 heterocycloalkyl, or substituted or unsubstituted monocyclic heteroaryl.
  • R 5 is -L'-I ⁇ -R 6 ;
  • L 2 is C r C 4 alkylene; substituted or
  • R 5 is -L'-R 7 ;
  • R 7 is substituted or unsubstituted monocyclic 5-membered or 6-membered C 2 -C 6 heterocycloalkyl, or substituted or unsubstituted monocyclic 5-membered or 6-membered heteroaryl.
  • R 4 is H, halogen, -CN, -OH, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 fluoroalkyl, substituted or unsubstituted Ci-C 6 fluoroalkoxy, or substituted or unsubstituted Ci-C 6 alkoxy;
  • each R 1 is independently selected from H, -OH, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 alkoxy, and substituted or unsubstituted C C 6 fiuoroalkyl;
  • R 1 are taken together with the carbon atom to which they are attached to form a substituted or unsubstituted C 3 -Ci 0 cycloalkyl or a substituted or unsubstituted C 2 - Cioheterocycloalkyl;
  • Ceheteroalkyl substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, substituted or unsubstituted phenyl or substituted or unsubstituted monocyclic heteroaryl;
  • ring B is 5-membered heteroaryl, bicyclic heteroaryl or naphthyl
  • n 0, 1, or 2;
  • R 4 is H, halogen, -CN, -N0 2 , -OH, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 fiuoroalkyl, substituted or unsubstituted Ci-C 6 fiuoroalkoxy, or substituted or unsubstituted Ci-C 6 alkoxy;
  • Cioheteroalkyl substituted or unsubstituted C3-Ciocycloalkyl, substituted or unsubstituted C 2 -Ci 0 heterocycloalkyl, substituted or unsubstituted phenyl, substituted or unsubstituted monocyclic heteroaryl, or -L 1 -L 2 -R 6 ;
  • L 2 is substituted or unsubstituted Ci-C 6 alkylene, substituted or unsubstituted C
  • each R 9 is independently selected from H, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 heteroalkyl, substituted or unsubstituted C C 6 fluoroalkyl, a substituted or unsubstituted C 3 -Ci 0 cycloalkyl, a substituted or unsubstituted C 2 -Cioheterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted benzyl, a substituted or unsubstituted heteroaryl, -Cr C 4 alkylene-(substituted or unsubstituted C 3 -Ci 0 cycloalkyl), -Ci-C 4 alkylene- (substituted or unsubstituted C 2 -Cioheterocycloalkyl), -Ci-C 4 alkylene-(substi
  • R 10 is substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Cr
  • C 6 heteroalkyl substituted or unsubstituted Ci-C 6 fiuoroaikyl, a substituted or unsubstituted C 3 -Ciocycloalkyl, a substituted or unsubstituted C 2 - Cioheterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted benzyl, a substituted or unsubstituted heteroaryl, -Ci-C 4 alkylene- (substituted or unsubstituted C 3 -Ciocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted C 2 -Ci 0 heterocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted aryl), or -Ci-C 4 alkylene-(substituted or unsubstituted hetero
  • R 11 is H or Ci-C 4 alkyl.
  • each R 1 is independently selected from H, -OH, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 alkoxy, and substituted or unsubstituted C
  • R 1 are taken together with the carbon atom to which they are attached to form a substituted or unsubstituted C 3 -C 6 cycloalkyl or a substituted or unsubstituted C 2 - C 6 heterocycloalkyl;
  • X is O or S
  • each R A is independently selected from H, halogen, -CN, -N0 2 , -OH, -OR 9 , -SR 9 , -
  • ring B is phenyl, naphthyl, monocyclic heteroaryl, or bicyclic heteroaryl;
  • n 0, 1, or 2;
  • L 2 is substituted or unsubstituted Ci-C 6 alkylene, substituted or unsubstituted C
  • each R 9 is independently selected from H, substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci-C 6 heteroalkyl, substituted or unsubstituted Ci- C 6 fluoroalkyl, a substituted or unsubstituted C 3 -Ci 0 cycloalkyl, a substituted or unsubstituted C 2 -Cioheterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted benzyl, a substituted or unsubstituted heteroaryl, -Ci- C 4 alkylene-(substituted or unsubstituted C 3 -Ci 0 cycloalkyl), -CrQalkylene- (substituted or unsubstituted C 2 -Cioheterocycloalkyl), -Ci-C 4 alkylene-(substi
  • R 10 is substituted or unsubstituted Ci-C 6 alkyl, substituted or unsubstituted Ci- C 6 heteroalkyl, substituted or unsubstituted Ci-C 6 fiuoroaikyl, a substituted or unsubstituted C 3 -Ciocycloalkyl, a substituted or unsubstituted C 2 - Cioheterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted benzyl, a substituted or unsubstituted heteroaryl, -Ci-C 4 alkylene- (substituted or unsubstituted C 3 -Ciocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted C 2 -Ci 0 heterocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstit
  • R 11 is H or Ci-C 4 alkyl.
  • L 2 is substituted or unsubstituted C C 6 alkylene, substituted or unsubstituted Ci-C 6 fluoroalkylene or substituted or unsubstituted Ci C 6 heteroalkylene;
  • each R A is independently selected from H, halogen, -CN, -N0 2 ,
  • both R 1 are taken together with the carbon atom to which they are attached to form a substituted or unsubstituted C 3 -C 6 cycloalkyl or a substituted or unsubstituted C 2 - C 6 heterocycloalkyl;
  • each R 1 is independently H, -OH, Ci-C 6 alkyl, Ci-C 6 alkoxy, or Ci-C 6 iluoroalkyl;
  • X is O or S
  • R A is C C 6 alkyl
  • ring B is phenyl, naphthyl, monocyclic heteroaryl, or bicyclic heteroaryl;
  • n 0, 1, or 2;
  • L 2 is Ci-C 6 alkylene, Ci-C 6 fluoroalkylene or Ci-C 6 heteroalkylene;
  • each R 9 is independently selected from H, Ci-C 6 alkyl, Ci-C 6 heteroalkyl, Ci-
  • C 6 fluoroalkyl a substituted or unsubstituted C 3 -Ci 0 cycloalkyl, a substituted or unsubstituted C 2 -Cioheterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted benzyl, a substituted or unsubstituted heteroaryl, -Ci- C 4 alkylene-(substituted or unsubstituted C 3 -Ci 0 cycloalkyl), -CrQalkylene- (substituted or unsubstituted C 2 -Cioheterocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted aryl), and -Ci-C 4 alkylene-(substituted or unsubstituted heteroaryl); or two R 9 groups attached to the same N atom are
  • R 10 is Ci-C 6 alkyl, Ci-C 6 heteroalkyl, Ci-C 6 fluoroalkyl, a substituted or unsubstituted C 3 - Ciocycloalkyl, a substituted or unsubstituted C 2 -Ci 0 heterocycloalkyl, a substituted or unsubstituted aryl, a substituted or unsubstituted benzyl, a substituted or unsubstituted heteroaryl, -Ci-C 4 alkylene-(substituted or unsubstituted C 3 - Ciocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted C 2 - Cioheterocycloalkyl), -Ci-C 4 alkylene-(substituted or unsubstituted aryl), or -Ci- C 4 alkylene-(substituted or unsubstituted
  • R 11 is H or C C 4 alkyl.
  • L 2 is C C 6 alkylene, d-Cefluoroalkylene or C C 6 heteroalkylene;
  • R 6 is -CN, -N0 2
  • R A is Ci-C 6 alkyl; both R 1 are taken together with the carbon atom to which they are attached to form a C3-C 6 cycloalkyl; or each R 1 is independently Cr
  • the compound of Formula (VIII) has the structure of Formula
  • each R A is independently selected from H, halogen, -OH, C C 6 alkyl, and Ci-C 6 alkoxy.
  • the compound of Formula (Villa) has the structure of Formula
  • each R 9 is independently selected from H, Ci-C 6 alkyl, Ci- C 6 heteroalkyl, Ci-C 6 fiuoroaikyl, a substituted or unsubstituted C 3 -C 6 cycloalkyl, a substituted or unsubstituted C 2 -C 6 heterocycloalkyl, a substituted or unsubstituted phenyl, a substituted or unsubstituted benzyl, and a substituted or unsubstituted monocyclic heteroaryl; or two R 9 groups attached to the same N atom are taken together with the N atom to which they are attached to form a substituted or unsubstituted C 2 -C 6 heterocycloalkyl; R is Ci-C 6 alkyl, C C 6 heteroalkyl, Ci-C 6 iluoroalkyl, a substituted or unsubstituted C3-C 6 cycloalkyl, a substituted or unsubstituted
  • R A is -CH 3 ; both R 1 are taken together with the carbon atom to which they are attached to form a cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl; or each R 1 is -CH 3 ;
  • L 2 is C C 4 alkylene;
  • R 6 is substituted or unsubstituted C 2 -C 6 heterocycloalkyl, substituted or unsubstituted monocyclic heteroaryl, or substituted or unsubstituted phenyl
  • the compound of Formula (VIII) or Formula (Villa) has the following structure:
  • R A is H, halogen, -OH, Ci-C 6 alkyl, or Ci-C 6 alkoxy. In some embodiments, R A is Ci-C 6 alkyl. In some embodiments, R A is -CH 3 .
  • R 4 is halogen.
  • R 4 is F.
  • each R 1 is independently selected from H and -CH 3 ;
  • R 1 are taken together with the carbon atom to which they are attached to form a cyclobutyl
  • X is O or S
  • X I is CH or N
  • each R 1 is independently selected from H and -CH 3 ;
  • R 1 are taken together with the carbon atom to which they are attached to form a cyclobutyl
  • X is O
  • X 1 is CH or N
  • each R 1 is independently selected from H and -CH 3 ;
  • R 1 are taken together with the carbon atom to which they are attached to form a cyclobutyl
  • X is O or S
  • X I is CH or N
  • compounds described herein include compounds in Table 1 , or a pharmaceutically acceptable salt thereof, or N-oxide thereof:
  • Compounds disclosed herein are AR modulators.
  • compounds disclosed herein are AR inverse agonists, AR antagonists, AR degraders, AR trafficking modulators and/or AR DNA-binding inhibitors.
  • compounds disclosed herein are AR inverse agonists.
  • compounds disclosed herein are AR antagonists.
  • compounds disclosed herein are AR degraders.
  • compounds disclosed herein are AR trafficking modulators.
  • compouds disclosed herein are AR DNA-binding inhibitors.
  • the overall profile of an AR modulator for the treatment of prostate cancer includes one or more of the foregoing profiles of an AR modulator.
  • compounds disclosed herein have the following properties: full AR antagonist in prostate cancer cells, inverse AR agonist in prostate cancer cells, no AR agonist activity in prostate cancer cells, AR Degrader activity in prostate cancer cells, no antagonist or agonist or degrader activity in non- prostate cancer cells, inhibition of prostate cancer growth.
  • compounds disclosed herein have the following properties: full AR antagonist in prostate cancer cells, inverse AR agonist in prostate cancer cells, no AR agonist activity in prostate cancer cells, AR Degrader activity in prostate cancer cells, and inhibition of prostate cancer growth.
  • compounds disclosed herein have the following properties: full AR antagonist in prostate cancer cells, inverse AR agonist in prostate cancer cells, no AR agonist activity in prostate cancer cells, inhibition of prostate cancer growth
  • compounds disclosed herein have the following properties: full AR antagonist in prostate cancer cells, no AR agonist activity in prostate cancer cells, inhibition of prostate cancer growth
  • compounds disclosed herein have the following properties: AR Trafficking Modulator, no AR agonist activity in prostate cancer cells, no antagonist or agonist or degrader activity in non- prostate cancer cells, inhibition of prostate cancer growth
  • compounds disclosed herein have the following properties: AR Trafficking Modulator, no AR agonist activity in prostate cancer cells, inhibition of prostate cancer growth.
  • the compound of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X) has minimal pro-convulsant activity and/or minimal impact on seizure threshold.
  • the compound of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X) displays minimal modulation of the GABA-gated chloride channel.
  • the compound of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X) displays minimal binding to the GABA-gated chloride channel.
  • the compound of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X) has minimal antagonism of the GABA-gated chloride channel.
  • the compound of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X) is an androgen receptor modulator with minimal interaction with a GABA-gated chloride channel.
  • the compound of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X) is an androgen receptor modulator with minimal interaction with the GABA A -gated chloride channel.
  • GABA assays are known and include, but are not limited to, those described in Ashok K. Mehta and Maharaj K. Ticku "Characterization of the Picrotoxin Site of GABA A Receptors" Current Protocols in Pharmacology (2000) 1.18.1-1.18.17; Copyright ⁇ 2000 by John Wiley & Sons, Inc., which is herein incorporated by reference.
  • a method of treating cancer in a mammal comprising administering to the mammal a thereapuetically effective amount of a compound, wherein the compound: a) is an androgen receptor inverse agonist; androgen receptor antagonist; is an androgen receptor degrader; is an androgen receptor trafficking modulator; is an androgen receptor DNA-binding inhibitor; or combinations thereof; and b) has minimal pro-convulsant activity and/or minimal impact on seizure threshold; displays minimal modulation of the GABA-gated chloride channel; displays minimal binding to the GABA-gated chloride channel; has minimal antagonism of the GABA-gated chloride channel; has minimal interaction with a GABA-gated chloride channel; or combinations thereof.
  • the compound has minimal interaction with the GABA A - gated chloride channel.
  • the cancer is prostate cancer.
  • the cancer is hormone refractory prostate cancer.
  • the compound is a compound of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X), or a pharmaceutically acceptable salt thereof or N-oxide thereof.
  • a method of identifying an androgen receptor modulator comprising: 1) testing a compound for androgen receptor modulatory activity in an appropriate assay; and 2) testing the same compound for activity on the GABA-gated chloride channel in an appropriate in vitro or in vivo assay; wherein the compound is an androgen receptor modulator if it exhibits activity in 1) and exhibits any one of the following in 2): displays minimal modulation of the GABA-gated chloride channel; displays minimal binding to the GABA-gated chloride channel; has minimal antagonism of the GABA-gated chloride channel; or has minimal interaction with the GABA-gated chloride channel.
  • the starting material used for the synthesis of the compounds of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) and (X) are either synthesized or obtained from commercial sources, such as, but not limited to, Sigma-Aldrich, Fluka, Acros Organics, Alfa Aesar, and the like.
  • the suitable solvent is acetic acid.
  • the reaction is performed at a temperature from about 25°C to about 80°C.
  • compounds of structure II are treated with thiophosgene and compounds of structure III in a suitable solvent, followed by treated with an acid to provide thiohydantions of structure IV.
  • the suitable solvent is
  • reaction is heated to about 60°C.
  • treatment with an acid encompasses treatment with hydrochloric acid.
  • treatment with an acid encompasses treatment with HCl, MeOH, at reflux for 2h.
  • compounds of structure V are elaborated into compounds of structure VI by reacting compounds of structure V with electrophiles or nucleophiles in the presence of a coupling agent.
  • compounds of structure V are treated with compounds such as R 6 -L 2 -OH in the presence of DIAD and PPh 3 in a suitable solvent to provide compounds of structure VI.
  • the suitable solvent is tetrahydrofurn.
  • esters of structure VII Treatment of esters of structure VII with a suitable base in a suitable solvent provides carboxylic acids of structure VIII.
  • the suitable base is lithium hydroxide.
  • the suitable solvent is tetrahydrofuran.
  • Carboxylic acids of structure VIII are then coupled with a variety of agents to provide compounds disclosed herein.
  • carboxylic acids of structure VIII are reated with amines R 6 -L 2 -NH 2 in the presence of a coupling reagent to provide amides of structure IX.
  • carboxylic acids of structure VIII are reated with alcohols R 6 -L 2 -OH in the presence of a coupling reagent to provide esters as described herein.
  • the coupling reagent is EDC, DCC, BOP, HATU or the like.
  • the coupling reaction is performed in a solvent selected from dichloromethane, dichloroethane, tetrahydrofuran, dimethoxyethane, dimethylformamide or the like in the presence of a base.
  • bases include, but are not limited to, triethylamine, diisopropylethylamine, N-methylmorpholine, pyridine or the like.
  • compounds of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) and (X) are synthesized as outlined in the Examples.
  • compounds of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) and (X) possess one or more stereocenters and each stereocenter exists independently in either the R or S configuration.
  • the compounds presented herein include all diastereomeric, enantiomeric, and epimeric forms as well as the appropriate mixtures thereof.
  • the compounds and methods provided herein include all cis, trans, syn, anti,
  • E Delta- ⁇
  • Z isomers
  • compounds of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) and (X) are prepared as their individual stereoisomers by reacting a racemic mixture of the compound with an optically active resolving agent to form a pair of diastereoisomeric compounds/salts, separating the diastereomers and recovering the optically pure enantiomers.
  • resolution of enantiomers is carried out using covalent diastereomeric derivatives of the compounds described herein.
  • diastereomers are seprated by separation/resolution techniques based upon differences in solubility.
  • separation of steroisomers is performed by chromatography or by the forming diastereomeric salts and separation by recrystallization, or chromatography, or any combination thereof.
  • stereoisomers are obtained by stereoselective synthesis.
  • compositions described herein include the use of amorphous forms as well as crystalline forms (also known as polymorphs).
  • compounds described herein are in the form of pharmaceutically acceptable salts.
  • active metabolites of these compounds having the same type of activity are included in the scope of the present disclosure.
  • the compounds described herein can exist in unsolvated as well as solvated forms with pharmaceutically acceptable solvents such as water, ethanol, and the like.
  • the solvated forms of the compounds presented herein are also considered to be disclosed herein.
  • prodrugs refers to an agent that is converted into the parent drug in vivo. Prodrugs are often useful because, in some situations, they may be easier to administer than the parent drug. They may, for instance, be bioavailable by oral administration whereas the parent is not. The prodrug may also have improved solubility in pharmaceutical compositions over the parent drug. In some embodiments, the design of a prodrug increases the effective water solubility.
  • a prodrug is a compound described herein, which is administered as an ester (the "prodrug") to facilitate transmittal across a cell membrane where water solubility is detrimental to mobility but which then is metabolically hydrolyzed to the carboxylic acid, the active entity, once inside the cell where water-solubility is beneficial.
  • a further example of a prodrug might be a short peptide (polyaminoacid) bonded to an acid group where the peptide is metabolized to reveal the active moiety.
  • a prodrug upon in vivo administration, a prodrug is chemically converted to the biologically, pharmaceutically or therapeutically active form of the compound.
  • a prodrug is
  • prodrugs are designed to alter the metabolic stability or the transport characteristics of a drug, to mask side effects or toxicity, to improve the flavor of a drug or to alter other characteristics or properties of a drug.
  • the design prodrugs of the compound is possible, (see, for example, Nogrady (1985) Medicinal Chemistry A Biochemical Approach, Oxford University Press, New York, pages 388-392; Silverman (1992), The Organic Chemistry of Drug Design and Drug Action, Academic Press, Inc., San Diego, pages 352-401, Rooseboom et ah, Pharmacological Reviews, 56:53-102, 2004; Aesop Cho, "Recent Advances in Oral Prodrug Discovery", Annual Reports in Medicinal Chemistry, Vol. 41, 395-407, 2006; T. Higuchi and V. Stella, Pro-drugs as Novel Delivery Systems, Vol. 14 of the A
  • Prodrug forms of the herein described compounds wherein the prodrug is metabolized in vivo to produce a compound of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X) as set forth herein are included within the scope of the claims.
  • some of the herein-described compounds may be a prodrug for another derivative or active compound.
  • sites on the aromatic ring portion of compounds of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) and (X) are susceptible to various metabolic reactions Therefore incorporation of appropriate substituents on the aromatic ring structures will reduce, minimize or eliminate this metabolic pathway.
  • the appropriate substituent to decrease or eliminate the susceptibility of the aromatic ring to metabolic reactions is, by way of example only, a halogen, or an alkyl group.
  • the compounds described herein are labeled isotopically (e.g. with a radioisotope) or by another other means, including, but not limited to, the use of chromophores or fluorescent moieties, bioluminescent labels, or chemiluminescent labels.
  • Compounds described herein include isotopically-labeled compounds, which are identical to those recited in the various formulae and structures presented herein, but for the fact that one or more atoms are replaced by an atom having an atomic mass or mass number different from the atomic mass or mass number usually found in nature.
  • isotopes that can be incorporated into the present compounds include isotopes of hydrogen, carbon, nitrogen, oxygen, fluorine and chlorine, such as, for example, 2 H, 3 H, 13 C, 14 C, 15 N, 18 0, 17 0, 35 S, 18 F, 36 C1.
  • isotopically-labeled compounds described herein for example those into which radioactive isotopes such as 3 H and 14 C are incorporated, are useful in drug and/or substrate tissue distribution assays.
  • substitution with isotopes such as deuterium affords certain therapeutic advantages resulting from greater metabolic stability, such as, for example, increased in vivo half-life or reduced dosage requirements.
  • the compounds described herein are metabolized upon administration to an organism in need to produce a metabolite that is then used to produce a desired effect, including a desired therapeutic effect.
  • “Pharmaceutically acceptable,” as used herein, refers a material, such as a carrier or diluent, which does not abrogate the biological activity or properties of the compound, and is relatively nontoxic, i.e., the material may be administered to an individual without causing undesirable biological effects or interacting in a deleterious manner with any of the components of the composition in which it is contained.
  • pharmaceutically acceptable salt refers to a formulation of a compound that does not cause significant irritation to an organism to which it is administered and does not abrogate the biological activity and properties of the compound.
  • pharmaceutically acceptable salts are obtained by reacting a compound of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X) with acids.
  • salts are also obtained by reacting a compound of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X) with a base to form a salt.
  • compositions described herein may be formed as, and/or used as, pharmaceutically acceptable salts.
  • pharmaceutical acceptable salts include, but are not limited to: (1) acid addition salts, formed by reacting the free base form of the compound with a
  • inorganic acid such as, for example, hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid, metaphosphoric acid, and the like
  • organic acid such as, for example, acetic acid, propionic acid, hexanoic acid
  • cyclopentanepropionic acid glycolic acid, pyruvic acid, lactic acid, malonic acid, succinic acid, malic acid, maleic acid, fumaric acid, trifluoroacetic acid, tartaric acid, citric acid, benzoic acid, 3-(4-hydroxybenzoyl)benzoic acid, cinnamic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, 1 ,2-ethanedisulfonic acid, 2-hydroxyethanesulfonic acid, benzenesulfonic acid, toluenesulfonic acid, 2-naphthalenesulfonic acid, 4-methylbicyclo-[2.2.2]oct-2-ene-l- carboxylic acid, glucoheptonic acid, 4,4'-methylenebis-(3-hydroxy-2-ene-l-carboxylic acid), 3- phenylpropionic acid, trimethylacetic acid, tertiary buty
  • compounds described herein may coordinate with an organic base, such as, but not limited to, ethanolamine, diethanolamine, triethanolamine, tromethamine, N-methylglucamine, dicyclohexylamine, tris(hydroxymethyl)methylamine.
  • compounds described herein may form salts with amino acids such as, but not limited to, arginine, lysine, and the like.
  • Acceptable inorganic bases used to form salts with compounds that include an acidic proton include, but are not limited to, aluminum hydroxide, calcium hydroxide, potassium hydroxide, sodium carbonate, sodium hydroxide, and the like.
  • a reference to a pharmaceutically acceptable salt includes the solvent addition forms or crystal forms thereof, particularly solvates or polymorphs.
  • Solvates contain either stoichiometric or non-stoichiometric amounts of a solvent, and may be formed during the process of crystallization with pharmaceutically acceptable solvents such as water, ethanol, and the like. Hydrates are formed when the solvent is water, or alcoholates are formed when the solvent is alcohol. Solvates of compounds described herein can be
  • the compounds provided herein can exist in unsolvated as well as solvated forms.
  • the solvated forms are considered equivalent to the unsolvated forms for the purposes of the compounds and methods provided herein.
  • Compounds described herein such as compounds of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) and (X), may be in various forms, including but not limited to, amorphous forms, milled forms and nano-particulate forms.
  • compounds described herein include crystalline forms, also known as polymorphs. Polymorphs include the different crystal packing arrangements of the same elemental composition of a compound.
  • Polymorphs usually have different X-ray diffraction patterns, melting points, density, hardness, crystal shape, optical properties, stability, and solubility. Various factors such as the recrystallization solvent, rate of crystallization, and storage temperature may cause a single crystal form to dominate.
  • alkyl refers to an aliphatic hydrocarbon group.
  • the alkyl group may be a saturated alkyl group or the the alkyl group may be an unsaturated alkyl group.
  • the alkyl moiety, whether saturated or unsaturated, may be branched or straight chain.
  • the "alkyl” group may have 1 to 10 carbon atoms (whenever it appears herein, a numerical range such as “1 to 10" refers to each integer in the given range; e.g. , "1 to 10 carbon atoms” means that the alkyl group may consist of 1 carbon atom, 2 carbon atoms, 3 carbon atoms, etc.
  • alkyl up to and including 10 carbon atoms, although the present definition also covers the occurrence of the term "alkyl” where no numerical range is designated).
  • the alkyl is selected from the group consisting of methyl, ethyl, propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, and t-butyl.
  • Typical alkyl groups include, but are in no way limited to, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tertiary butyl, pentyl, neopentyl, hexyl, allyl, but-2-enyl, but-3-enyl, and the like.
  • an alkyl is a Ci-C 6 alkyl.
  • alkylene refers to a divalent alkyl radical. Any of the above mentioned monovalent alkyl groups may be an alkylene by abstraction of a second hydrogen atom from the alkyl. In one aspect, an alkelene is a Ci-Cioalkylene. In another apsect, an alkylene is a Ci- C 6 alkylene.
  • Typical alkylene groups include, but are not limited to, -CH 2 -, -CH(CH 3 )-, - C(CH 3 ) 2 -, -CH 2 CH 2 -, -CH 2 CH(CH 3 )-, -CH 2 C(CH 3 ) 2 -, -CH 2 CH 2 CH 2 -, -CH 2 CH 2 CH 2 CH 2 -, - CH 2 CH 2 CH 2 CH 2 -, -CH 2 CH 2 CH 2 CH 2 CH 2 -, and the like.
  • alkoxy group refers to a (alkyl)O- group, where alkyl is as defined herein.
  • aromatic refers to a planar ring having a delocalized ⁇ -electron system containing 4n+2 ⁇ electrons, where n is an integer. Aromatic rings can be formed from five, six, seven, eight, nine, ten, or more than ten atoms. Aromatics are optionally substituted.
  • aromatic includes both carbocyclic aryl ("aryl”, e.g., phenyl) and heterocyclic aryl (or “heteroaryl” or “heteroaromatic”) groups ⁇ e.g., pyridine).
  • aryl e.g., phenyl
  • heterocyclic aryl or “heteroaryl” or “heteroaromatic” groups ⁇ e.g., pyridine.
  • the term includes monocyclic or fused-ring polycyclic ⁇ i.e., rings which share adjacent pairs of carbon atoms) groups.
  • Carbocyclic or “carbocycle” refers to a ring or ring system where the atoms forming the backbone of the ring are all carbon atoms. The term thus distinguishes carbocyclic from heterocyclic rings in which the ring backbone contains at least one atom which is different from carbon.
  • aryl refers to an aromatic ring wherein each of the atoms forming the ring is a carbon atom.
  • Aryl rings are formed by five, six, seven, eight, nine, or more than nine carbon atoms.
  • Aryl groups are optionally substituted.
  • an aryl is a phenyl or a naphthalenyl.
  • an aryl is a phenyl.
  • an aryl is a C6-Cioaryl.
  • an aryl group can be a monoradical or a diradical (i.e., an arylene group).
  • Examplary arylenes include, but are not limited to, phenyl- 1 ,2-ene, phenyl- 1 , 3 -ene, and phenyl- 1 ,4-ene.
  • cycloalkyl refers to a monocyclic or polycyclic aliphatic, non-aromatic radical, wherein each of the atoms forming the ring (i.e. skeletal atoms) is a carbon atom.
  • Cycloalkyls may be saturated, or partially unsaturated. Cycloalkyls may be fused with an aromatic ring, and the point of attachment is at a carbon that is not an aromatic ring carbon atom. Cycloalkyl groups include groups having from 3 to 10 ring atoms. In some embodiments, cycloalkyl groups are selected from among cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl, cycloheptyl, and cyclooctyl. Cycloalkyl groups may be substituted or unsubstituted.
  • a cycloalkyl group can be a monoradical or a diradical (i.e., an cycloalkylene group, such as, but not limited to, cyclopropan- 1 , 1 -diyl, cyclobutan-l ,l-diyl, cyclopentan- 1 ,1 -diyl, cyclohexan- 1 ,1 -diyl, cyclohexan-l ,4-diyl, cycloheptan- 1 ,1 -diyl, and the like).
  • a cycloalkyl is a C 3 -C 6 cycloalkyl.
  • halo or, alternatively, "halogen” or “halide” means fluoro, chloro, bromo or iodo.
  • haloalkyl refers to an alkyl group in which one or more hydrogen atoms are replaced by one or more halide atoms.
  • a haloalkyl is a Ci-C 6 haloalkyl.
  • haloalkylene refers to an alkylene group in which one or more hydrogen atoms are replaced by one or more halide atoms.
  • a haloalkylene is a Cp
  • fluoroalkyl refers to an alkyl in which one or more hydrogen atoms are replaced by a fluorine atom.
  • a fluoralkyl is a Ci-C 6 fiuoroalkyl.
  • fluoroalkylene refers to an alkylene in which one or more hydrogen atoms are replaced by a fluorine atom.
  • a fluoralkyl ene is a Ci-C 6 fluoroalkylene.
  • heteroalkyl refers to an alkyl group in which one or more skeletal atoms of the alkyl are selected from an atom other than carbon, e.g. , oxygen, nitrogen (e.g. -NH-, - N(alkyl)-, sulfur, or combinations thereof.
  • a heteroalkyl is a Ci-Ceheteroalkyl.
  • heteroalkylene refers to an alkylene group in which one or more skeletal atoms of the alkyl are selected from an atom other than carbon, e.g. , oxygen, nitrogen, sulfur, phosphorus or combinations thereof.
  • a heteroalkylene is a Ci-Ceheteroalkylene.
  • Examplary heteroalkylenes include, but are not limited to, -OCH 2 -, -OCH(CH 3 )-, -OC(CH 3 ) 2 -, - OCH 2 CH 2 -, -OCH 2 CH 2 CH 2 -, -CH 2 0-, -CH(CH 3 )0-, -C(CH 3 ) 2 0-, -CH 2 CH 2 0-, -CH 2 OCH 2 -, - CH 2 OCH 2 CH 2 -, -CH 2 CH 2 OCH 2 -, -SCH 2 -, -SCH(CH 3 )-, -SC(CH 3 ) 2 -, -SCH 2 CH 2 -, -CH 2 S-, - CH(CH 3 )S-, -C(CH 3 ) 2 S-, -CH 2 CH 2 S-, -CH 2 SCH 2 -, -CH 2 SCH 2 CH 2 -, -CH 2 CH 2 -, -CH 2 CH
  • heterocycle refers to heteroaromatic rings (also known as heteroaryls) and heterocycloalkyl rings (also known as heteroalicyclic groups) containing one to four heteroatoms in the ring(s), where each heteroatom in the ring(s) is selected from O, S and N, wherein each heterocyclic group has from 4 to 10 atoms in its ring system, and with the proviso that the any ring does not contain two adjacent O or S atoms.
  • Non-aromatic heterocyclic groups also known as heterocycloalkyls
  • the heterocyclic groups include benzo-fused ring systems.
  • An example of a 3-membered heterocyclic group is aziridinyl.
  • An example of a 4-membered heterocyclic group is azetidinyl.
  • An example of a 5-membered heterocyclic group is thiazolyl.
  • An example of a 6-membered heterocyclic group is pyridyl, and an example of a 10-membered heterocyclic group is quinolinyl.
  • non-aromatic heterocyclic groups are pyrrolidinyl, tetrahydrofuranyl, dihydrofuranyl, tetrahydrothienyl, oxazolidinonyl, tetrahydropyranyl, dihydropyranyl, tetrahydrothiopyranyl, piperidinyl, morpholinyl, thiomorpholinyl, thioxanyl, piperazinyl, aziridinyl, azetidinyl, oxetanyl, thietanyl, homopiperidinyl, oxepanyl, thiepanyl, oxazepinyl, diazepinyl, thiazepinyl, 1 ,2,3,6-tetrahydropyridinyl, pyrrolin-2-yl, pyrrolin-3-yl, indolinyl, 2H- pyranyl, 4H-pyranyl, diox
  • aromatic heterocyclic groups are pyridinyl, imidazolyl, pyrimidinyl, pyrazolyl, triazolyl, pyrazinyl, tetrazolyl, furyl, thienyl, isoxazolyl, thiazolyl, oxazolyl, isothiazolyl, pyrrolyl, quinolinyl, isoquinolinyl, indolyl, benzimidazolyl, benzofuranyl, cinnolinyl, indazolyl, indolizinyl, phthalazinyl, pyridazinyl, triazinyl, isoindolyl, pteridinyl, purinyl, oxadiazolyl, thiadiazolyl, furazanyl, benzofurazanyl, benzothiophenyl, benzothiazolyl, benzoxazolyl, quinazolinyl, quinox
  • the foregoing groups may be C- attached (or C-linked) or N-attached where such is possible.
  • a group derived from pyrrole may be pyrrol- 1-yl (N-attached) or pyrrol-3-yl (C-attached).
  • a group derived from imidazole may be imidazol- 1 -yl or imidazol-3-yl (both N-attached) or imidazol-2-yl, imidazol-4-yl or imidazol-5-yl (all C-attached).
  • heteroaryl or, alternatively, “heteroaromatic” refers to an aryl group that includes one or more ring heteroatoms selected from nitrogen, oxygen and sulfur.
  • heteroaryl groups include the following moieties:
  • heteroaryls include pyridinyl, imidazolyl, pyrimidinyl, pyrazolyl, triazolyl, pyrazinyl, tetrazolyl, furyl, thienyl, isoxazolyl, thiazolyl, oxazolyl, isothiazolyl, pyrrolyl, pyridazinyl, triazinyl, oxadiazolyl, thiadiazolyl, and furazanyl.
  • a heteroaryl contains 0-3 N atoms in the ring. In some embodiments, a heteroaryl contains 1 -3 N atoms in the ring.
  • a heteroaryl contains 0-3 N atoms, 0-1 O atoms, and 0-1 S atoms in the ring.
  • a heteroaryl is a monocyclic or bicyclic heteroaryl.
  • heteroaryl is a Ci-Cgheteroaryl.
  • monocyclic heteroaryl is a Ci- Csheteroaryl.
  • monocyclic heteroaryl is a 5-membered or 6-membered heteroaryl.
  • bicyclic heteroaryl is a Ce-Cgheteroaryl.
  • a heteroaryl group can be a monoradical or a diradical (i.e., a heteroarylene group).
  • heterocycloalkyl or “heteroalicyclic” group refers to a cycloalkyl group that includes at least one heteroatom selected from nitrogen, oxygen and sulfur.
  • the radicals may be fused with an aryl or heteroaryl.
  • heterocycloalkyl groups also referred to
  • the heterocycloalkyl is selected from oxazolidinonyl, pyrrolidinyl, tetrahydrofuranyl, tetrahydrothienyl, tetrahydropyranyl, tetrahydrothiopyranyl, piperidinyl, morpholinyl, thiomorpholinyl, piperazinyl, and indolinyl.
  • the heterocycloalkyl is pyrrolidinyl, tetrahydrofuranyl, tetrahydrothienyl, tetrahydropyranyl, tetrahydrothiopyranyl, piperidinyl, morpholinyl, thiomorpholinyl, or piperazinyl.
  • the term heteroahcyclic also includes all ring forms of the carbohydrates, including but not limited to the monosaccharides, the disaccharides and the oligosaccharides.
  • a heterocycloalkyl is a C2-Cioheterocycloalkyl.
  • a heterocycloalkyl is a C4-Cioheterocycloalkyl. In some embodiments, a heterocycloalkyl contains 0-2 N atoms in the ring. In some embodiments, a heterocycloalkyl contains 0-2 N atoms, 0-2 O atoms and 0-1 S atoms in the ring.
  • bond refers to a chemical bond between two atoms, or two moieties when the atoms joined by the bond are considered to be part of larger substructure.
  • bond when a group described herein is a bond, the referenced group is absent thereby allowing a bond to be formed between the remaining identified groups.
  • moiety refers to a specific segment or functional group of a molecule.
  • Chemical moieties are often recognized chemical entities embedded in or appended to a molecule.
  • carboxylic acid bioisostere refers to a functional group or moiety that exhibits similar physical, biological and/or chemical properties as a carboxylic acid moiety.
  • Examples of carboxylic acid bioisosteres include, but are not limited to,
  • the term "optionally substituted” or “substituted” means that the referenced group may be substituted with one or more additional group(s) individually and independently selected from alkyl, cycloalkyl, aryl, heteroaryl, heteroahcyclic, hydroxy, alkoxy, aryloxy, alkylthio, arylthio, alkylsulfoxide, arylsulfoxide, alkylsulfone, arylsulfone, cyano, halo, nitro, haloalkyl, fluoroalkyl, fluoroalkoxy, and amino, including mono- and di-substituted amino groups, and the protected derivatives thereof.
  • optional substituents are independently selected from halogen, -CN, - NH 2 , -NH(CH 3 ), -N(CH 3 ) 2 , -OH, alkyl, fluoroalkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, alkoxy, aryloxy, alkylthio, arylthio, alkylsulfoxide, arylsulfoxide, alkylsulfone, and arylsulfone.
  • optional substituents are independently selected from halogen, -CN, -NH 2 , -OH, - NH(CH 3 ), -N(CH 3 ) 2 , -CH 3 , -CH 2 CH 3 , -CF 3 , -CH 2 CF 3 , -OCH 3 , -OCH 2 CH 3 , and -OCF 3 .
  • substituted groups are substituted with one or two of the preceding groups.
  • the compounds presented herein possess one or more stereocenters and each center independently exists in either the R or S configuration.
  • the compounds presented herein include all diastereomeric, enantiomeric, and epimeric forms as well as the appropriate mixtures thereof.
  • Stereoisomers are obtained, if desired, by methods such as, stereoselective synthesis and/or the separation of stereoisomers by chiral
  • the methods and formulations described herein include the use of N-oxides (if appropriate), crystalline forms (also known as polymorphs), or pharmaceutically acceptable salts of compounds having the structure of Formula (I), (la), (II), (III), (IV), (V), (VI), (VII), (VIII), (Villa), (IX), (IXa) or (X), as well as active metabolites of these compounds having the same type of activity.
  • compounds may exist as tautomers. All tautomers are included within the scope of the compounds presented herein.
  • the compounds described herein exist in solvated forms with pharmaceutically acceptable solvents such as water, ethanol, and the like. In other embodiments, the compounds described herein exist in unsolvated form.
  • modulate means to interact with a target either directly or indirectly so as to alter the activity of the target, including, by way of example only, to enhance the activity of the target, to inhibit the activity of the target, to limit the activity of the target, or to extend the activity of the target.
  • modulator refers to a molecule that interacts with a target either directly or indirectly. The interactions include, but are not limited to, the interactions of an agonist, partial agonist, an inverse agonist, antagonist, degrader, AR trafficking modulator, AR DNA-binding inhibitor.
  • a modulator is an antagonist.
  • a modulator is an inverse agonist, antagonist, degrader, AR trafficking modulator and/or a DNA binding inhibitor.
  • antagonist refers to a small -molecule agent that binds to a nuclear hormone receptor and subsequently decreases the agonist induced transcriptional activity of the nuclear hormone receptor.
  • agonist refers to a small-molecule agent that binds to a nuclear hormone receptor and subsequently increases nuclear hormone receptor transcriptional activity in the absence of a known agonist.
  • inverse agonist refers to a small-molecule agent that binds to a nuclear hormone receptor and subsequently decreases the basal level of nuclear hormone receptor transcriptional activity that is present in the absence of a known agonist.
  • degradation refers to a small molecule agent that binds to a nuclear hormone receptor and subsequently lowers the steady state protein levels of said receptor.
  • AR trafficking modulator refers to a small-molecule agent that binds to a nuclear hormone receptor and subsequently alters the normal subcellular location of the receptor thereby interfering with its function and signaling.
  • DNA-binding inhibitor refers to a small-molecule agent that binds to a nuclear hormone receptor and subsequently prevents DNA binding of the receptor thereby interfering with its function and signaling.
  • AR-dependent refers to diseases or conditions that would not occur, or would not occur to the same extent, in the absence of androgen receptors.
  • AR-mediated refers to diseases or conditions that might occur in the absence of androgen receptors but can occur in the presence of androgen receptors.
  • Selective with respect to androgen receptors means that the compound preferentially binds to androgen receptors versus other nuclear receptors.
  • a selective androgen receptor modulator preferentially binds to androgen receptors and displays little, if any, affinity to other nuclear receptors.

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Abstract

Les composés ci-décrits sont des modulateurs du récepteur des androgènes. Des compositions pharmaceutiques et des médicaments contenant les composés ci-décrits, ainsi que des procédés d'utilisation de ces modulateurs du récepteur des androgènes, seuls et en combinaison avec d'autres composés, pour traiter les maladies ou les affections qui sont médiées ou dépendent du récepteur des androgènes sont également décrits.
EP11745183.1A 2010-02-16 2011-02-16 Modulateurs du récepteur des androgènes et leurs utilisations Withdrawn EP2536708A4 (fr)

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PL16184263T PL3124481T3 (pl) 2010-02-16 2011-02-16 Modulatory receptora androgenowego i ich zastosowanie
EP18161153.4A EP3357917A1 (fr) 2010-02-16 2011-02-16 Modulateurs de récepteur d'androgène et utilisations associées
EP16184263.8A EP3124481B1 (fr) 2010-02-16 2011-02-16 Modulateurs de récepteur d'androgène et utilisations associées
EP14188300.9A EP2824102B1 (fr) 2010-02-16 2011-02-16 Modulateurs de récepteur d'androgène et utilisations associées
CY20181100592T CY1120297T1 (el) 2010-02-16 2018-06-06 Ρυθμιστες υποδοχεα ανδρογονου και χρησεις αυτων

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Families Citing this family (65)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HUE037389T2 (hu) 2010-02-16 2018-08-28 Aragon Pharmaceuticals Inc Androgén receptor modulátorok és alkalmazásaik
WO2012119559A1 (fr) 2011-03-10 2012-09-13 Suzhou Kintor Pharmaceuticals,Inc. Antagonistes des récepteurs d'androgènes et leurs utilisations
WO2013056547A1 (fr) * 2011-10-22 2013-04-25 Chen Degui Synthèse du dérivé de l'hydantoïne et ses applications
EA201490897A1 (ru) 2011-12-16 2015-03-31 Олема Фармасьютикалс, Инк. Новые бензопирановые соединения, композиции и их применение
TWI635080B (zh) 2012-01-13 2018-09-11 阿蘭達製藥有限公司 具抗雄激素性質新雜芳醯胺衍生物及其用途
UY34646A (es) 2012-03-02 2013-10-31 Novartis Ag Compuestos de espirohidantoína y su uso como moduladores selectivos del receptor de andrógenos
EP3922629A1 (fr) * 2012-06-07 2021-12-15 Aragon Pharmaceuticals, Inc. Formes cristallines d'un modulateur de récepteur d'androgène
ES2836424T3 (es) 2012-09-26 2021-06-25 Aragon Pharmaceuticals Inc Antiandrógenos para tratar el cáncer de próstata no metastásico y resistente a la castración
US9175291B2 (en) 2012-10-11 2015-11-03 Isis Pharmaceuticals Inc. Modulation of androgen receptor expression
WO2014075387A1 (fr) * 2012-11-14 2014-05-22 上海医药集团股份有限公司 Dérivé de diaryl hydantoïne, et procédé de préparation, composition pharmaceutique et utilisation associée
CA3105575A1 (fr) 2013-01-15 2014-07-24 Aragon Pharmaceuticals, Inc. Modulateur du recepteur des androgenes et ses utilisations
CA2908326C (fr) 2013-05-29 2017-09-12 Hinova Pharmaceuticals Inc. Composes d'imidazolidinedione et leurs utilisations
WO2015018356A1 (fr) * 2013-08-08 2015-02-12 上海医药集团股份有限公司 Dérivé de diarylhydantoïne et procédé de préparation, composition pharmaceutique et utilisation correspondants
CN103601671B (zh) * 2013-10-22 2016-08-17 上海泰坦科技股份有限公司 碘代三氟甲基吡啶的制备方法
US9682960B2 (en) 2013-12-19 2017-06-20 Endorecherche, Inc. Non-steroidal antiandrogens and selective androgen receptor modulators with a pyridyl moiety
CN103694243B (zh) * 2013-12-20 2015-09-09 中国农业大学 2-取代吡啶基-1,2,4-三唑并[1,2-a]哒嗪化合物
WO2015116696A1 (fr) 2014-01-28 2015-08-06 Massachusetts Institute Of Technology Thérapies de combinaison et procédés d'utilisation associés pour le traitement du cancer
EP3102183A1 (fr) * 2014-02-05 2016-12-14 LEK Pharmaceuticals d.d. Compositions pharmaceutiques solides d'antagonistes du récepteur des androgènes
CN104844520B (zh) * 2014-02-13 2017-09-05 成都伊诺达博医药科技有限公司 一种合成恩杂鲁胺的方法
CN104844521B (zh) * 2014-02-13 2017-08-15 成都伊诺达博医药科技有限公司 抗前列腺癌药物恩杂鲁胺的合成方法
RU2557235C1 (ru) * 2014-07-08 2015-07-20 Александр Васильевич Иващенко Замещенные 2-тиоксо-имидазолидин-4-оны и их спироаналоги, противораковый активный компонент, фармацевтическая композиция, лекарственный препарат, способ лечения рака простаты
MX381829B (es) 2014-12-05 2025-03-13 Aragon Pharmaceuticals Inc Composiciones anticancerígenas.
ES2839128T3 (es) * 2014-12-05 2021-07-05 Aragon Pharmaceuticals Inc Composiciones anticancerosas
RS66323B1 (sr) 2014-12-05 2025-01-31 Aragon Pharmaceuticals Inc Sastavi protiv raka
ME03420B (fr) * 2014-12-19 2020-01-20 Aragon Pharmaceuticals Inc Procédé pour la préparation d'un composé diarylthiohydantoïne
EP3233823B1 (fr) * 2014-12-19 2019-01-30 Aragon Pharmaceuticals, Inc. Procédés pour la préparation d'un composé diaryl-thiohydantoïne
US12312316B2 (en) 2015-01-20 2025-05-27 Arvinas Operations, Inc. Compounds and methods for the targeted degradation of androgen receptor
MX390189B (es) * 2015-01-20 2025-03-20 Arvinas Operations Inc COMPUESTOS Y METODOS PARA LA DEGRADACION DIRIGIDA DE RECEPTOR DE ANDROGENOs.
CN105732575A (zh) * 2015-02-06 2016-07-06 苏州晶云药物科技有限公司 一种治疗前列腺癌的新型抗雄激素类药物的新晶型及其制备方法
TWI698430B (zh) 2015-02-13 2020-07-11 南北兄弟藥業投資有限公司 三環化合物及其在藥物中的應用
US10471023B2 (en) 2015-03-12 2019-11-12 British Columbia Cancer Agency Branch Bisphenol ether derivatives and methods for using the same
RU2019115778A (ru) * 2015-04-21 2019-06-24 Джи Ти Икс, ИНК. Селективные лиганды - разрушители андрогенных рецепторов (sard) и способы их применения
US10093613B2 (en) 2015-04-21 2018-10-09 Gtx, Inc. Selective androgen receptor degrader (SARD) ligands and methods of use thereof
US10865184B2 (en) 2015-04-21 2020-12-15 University Of Tennessee Research Foundation Selective androgen receptor degrader (SARD) ligands and methods of use thereof
US10654809B2 (en) 2016-06-10 2020-05-19 University Of Tennessee Research Foundation Selective androgen receptor degrader (SARD) ligands and methods of use thereof
US10441570B2 (en) 2015-04-21 2019-10-15 University Of Tennessee Research Foundation Selective androgen receptor degrader (SARD) Ligands and methods of use thereof
US10806720B2 (en) 2015-04-21 2020-10-20 University Of Tennessee Research Foundation Selective androgen receptor degrader (SARD) ligands and methods of use thereof
BR112017027339A2 (pt) 2015-06-18 2018-09-04 Cephalon, Inc. derivados de piperidina 1,4-substituída
US10919875B2 (en) 2015-06-18 2021-02-16 89Bio Ltd Substituted 4-benzyl and 4-benzoyl piperidine derivatives
TWI726969B (zh) * 2016-01-11 2021-05-11 比利時商健生藥品公司 用作雄性激素受體拮抗劑之經取代之硫尿囊素衍生物
US20170298033A1 (en) 2016-04-15 2017-10-19 The University Of British Columbia Bisphenol derivatives and their use as androgen receptor activity modulators
WO2018009694A1 (fr) 2016-07-08 2018-01-11 Janssen Pharmaceutica Nv Antagonistes du récepteur des androgènes thiohydantoïne pour le traitement du cancer
CA3034449A1 (fr) * 2016-08-22 2018-03-01 Janssen Pharmaceutica Nv Antagonistes du recepteur des androgenes thiohydantoine pour le traitement du cancer
CN108069869B (zh) * 2016-11-09 2022-03-01 上海医药工业研究院 一种Apalutamide的制备方法及其中间体
EP3555061B1 (fr) * 2016-12-13 2023-06-07 Watson Laboratories Inc. Formes à l'état solide de l'apalutamide
US11332465B2 (en) 2017-08-07 2022-05-17 Chia Tai Tianqing Pharmaceutical Group Co., Ltd. Diarylthiohydantoin compound as androgen receptor antagonist
CN109422737B (zh) * 2017-08-22 2021-07-30 上海时莱生物技术有限公司 咪唑酮类雄激素受体拮抗剂、其制备方法和用途
CN111479805B (zh) * 2017-08-29 2024-08-13 罗格斯新泽西州立大学 治疗性吲唑
CN109422725A (zh) * 2017-09-04 2019-03-05 北京美倍他药物研究有限公司 前列腺癌治疗药物
UA129105C2 (uk) 2017-10-16 2025-01-15 Арагон Фармасьютикалз, Інк. Антиандрогени для лікування неметастатичного резистентного до кастрації раку передміхурової залози
CN107987055A (zh) * 2017-12-19 2018-05-04 刘秀云 硫代咪唑二酮类雄激素受体拮抗剂及其用途
US10513504B2 (en) 2018-03-08 2019-12-24 Apotex Inc. Processes for the preparation of apalutamide and intermediates thereof
WO2020051344A1 (fr) 2018-09-05 2020-03-12 University Of Tennessee Research Foundation Ligands de composés de dégradation sélectifs de récepteurs des androgènes (sard) et procédés d'utilisation associés
EP3886854A4 (fr) 2018-11-30 2022-07-06 Nuvation Bio Inc. Composés pyrrole et pyrazole et leurs procédés d'utilisation
US11292782B2 (en) 2018-11-30 2022-04-05 Nuvation Bio Inc. Diarylhydantoin compounds and methods of use thereof
US12358913B2 (en) 2019-02-01 2025-07-15 Chia Tai Tianqing Pharmaceutical Group Co., Ltd. Crystal of diarylthiohydantoin compound
US12109179B2 (en) 2019-03-28 2024-10-08 Essa Pharma Inc. Pharmaceutical compositions and combinations comprising inhibitors of the androgen receptor and uses thereof
CN110452166A (zh) * 2019-09-06 2019-11-15 浙江朗华制药有限公司 一种5-异硫氰酰基-3-三氟甲基-2-氰基吡啶的制备方法
TW202122382A (zh) * 2019-09-06 2021-06-16 日商小野藥品工業股份有限公司 乙內醯脲衍生物
JP2023522040A (ja) 2020-04-17 2023-05-26 エッサ ファーマ，インコーポレイテッド Ｎ末端ドメインアンドロゲン受容体阻害剤の固体形態およびその使用
CN113698317B (zh) * 2020-05-20 2025-09-30 苏州科伦药物研究有限公司 阿帕他胺的合成方法、其中间体及合成方法
CN114315805A (zh) * 2020-10-09 2022-04-12 中国科学院上海药物研究所 芳环并环状内脂类硫代乙内酰脲化合物及制备方法和用途
WO2022226349A1 (fr) * 2021-04-22 2022-10-27 Essa Pharma, Inc. Modulateurs du récepteur des androgènes et leurs procédés d'utilisation
CN115650954A (zh) * 2022-10-24 2023-01-31 江苏海悦康医药科技有限公司 阿帕他胺有关物质的制备方法
WO2024088395A1 (fr) * 2022-10-28 2024-05-02 南京明德新药研发有限公司 Composé cyclique ponté et son utilisation pharmaceutique

Family Cites Families (128)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3823240A (en) 1970-10-06 1974-07-09 Rhone Poulenc Sa Fungicidal hydantoin derivatives
GB1472467A (en) 1974-04-19 1977-05-04 Wyeth John & Brother Ltd Thiohydantoins
FR2329276A1 (fr) 1975-10-29 1977-05-27 Roussel Uclaf Nouvelles imidazolidines substituees, procede de preparation, application comme medicament et compositions les renfermant
DE2614831A1 (de) 1976-04-06 1977-10-20 Bayer Ag 1,3,4-thiadiazolylderivate, verfahren zu ihrer herstellung sowie ihre verwendung als herbizide
MC1220A1 (fr) 1977-10-28 1979-07-20 Hoffmann La Roche Nouveaux derives d'imidazolidine
IL55774A (en) 1977-10-28 1982-04-30 Sparamedica Ag Pharmaceutical compositions containing urea derivatives,certain such novel derivatives and their manufacture
JPS5492962A (en) 1977-12-01 1979-07-23 Wellcome Found Thiohydantoin compound
EP0004723A1 (fr) 1978-03-30 1979-10-17 Beecham Group Plc Déoxyhydantoines, leurs procédés de préparation et compositions pharmaceutiques les contenant
FR2449448B1 (fr) 1979-02-20 1983-05-27 Inst Nat Radio Elements Composition pharmaceutique comprenant un derive de phenylhydantoine, derives mis en oeuvre et leur preparation
FI801184A7 (fi) 1979-04-24 1981-01-01 F Hoffmann La Roche & Co Menetelmä imidatsolidiini-johdannaisten valmistamiseksi.
US4229447A (en) 1979-06-04 1980-10-21 American Home Products Corporation Intraoral methods of using benzodiazepines
US4399216A (en) 1980-02-25 1983-08-16 The Trustees Of Columbia University Processes for inserting DNA into eucaryotic cells and for producing proteinaceous materials
JPS57197268A (en) 1981-05-29 1982-12-03 Sumitomo Chem Co Ltd Substituted phenylhydantoin derivative, its preparation, and herbicide containing the same as active ingredient
EP0091596B1 (fr) 1982-04-08 1991-09-11 Shell Internationale Researchmaatschappij B.V. Hydantoins, préparation et application
US4473393A (en) 1982-08-06 1984-09-25 Buffalo Color Corporation Pesticidal thiohydantoin compositions
US4559157A (en) 1983-04-21 1985-12-17 Creative Products Resource Associates, Ltd. Cosmetic applicator useful for skin moisturizing
JPS59210083A (ja) 1983-05-13 1984-11-28 Otsuka Chem Co Ltd １，３，４−チアジアゾ−ル−５−オン誘導体、その製造法及び該誘導体を有効成分とする除草剤
LU84979A1 (fr) 1983-08-30 1985-04-24 Oreal Composition cosmetique ou pharmaceutique sous forme aqueuse ou anhydre dont la phase grasse contient un polyether oligomere et polyethers oligomeres nouveaux
JPS6092285A (ja) 1983-10-26 1985-05-23 Shionogi & Co Ltd イソオキサゾ−ル系環状尿素類
US4596795A (en) 1984-04-25 1986-06-24 The United States Of America As Represented By The Secretary, Dept. Of Health & Human Services Administration of sex hormones in the form of hydrophilic cyclodextrin derivatives
JPH0778017B2 (ja) 1985-12-28 1995-08-23 住友製薬株式会社 パルス的かつ持続放出性製剤
US4755386A (en) 1986-01-22 1988-07-05 Schering Corporation Buccal formulation
DE3604042A1 (de) 1986-02-08 1987-08-13 Hoechst Ag Imidazolidin(thi)on-derivate, verfahren zu ihrer herstellung sowie ihre verwendung im pflanzenschutz
US5071773A (en) 1986-10-24 1991-12-10 The Salk Institute For Biological Studies Hormone receptor-related bioassays
US4820508A (en) 1987-06-23 1989-04-11 Neutrogena Corporation Skin protective composition
JPS649978A (en) 1987-07-02 1989-01-13 Shionogi & Co Perfluoroalkylisoxazole derivative
US4859228A (en) 1987-07-16 1989-08-22 Ici Americas Inc Novel 5-aminomethylene-2,4-imidazolidinediones and 5-aminomethylene-2-thionoimidazolidine-4-ones
US5010182A (en) 1987-07-28 1991-04-23 Chiron Corporation DNA constructs containing a Kluyveromyces alpha factor leader sequence for directing secretion of heterologous polypeptides
FR2619381B1 (fr) 1987-08-13 1989-12-08 Roussel Uclaf Nouvelles imidazolidines substituees par un radical hydroxymethyle et un radical phenyl substitue, leur procede de preparation, leur application comme medicaments, les compositions pharmaceutiques les renfermant et un intermediaire pour leur preparation
US5033252A (en) 1987-12-23 1991-07-23 Entravision, Inc. Method of packaging and sterilizing a pharmaceutical product
US5052558A (en) 1987-12-23 1991-10-01 Entravision, Inc. Packaged pharmaceutical product
CA1331757C (fr) 1988-02-29 1994-08-30 Janssen Pharmaceutica Naamloze Vennootschap 5-lipoxygenase inhibant les 4-(4-phenyl-1-piperazinyl)phenols
US5614620A (en) 1988-03-30 1997-03-25 Arch Development Corporation DNA binding proteins including androgen receptor
US4992478A (en) 1988-04-04 1991-02-12 Warner-Lambert Company Antiinflammatory skin moisturizing composition and method of preparing same
US6307030B1 (en) 1988-04-15 2001-10-23 The University Of North Carolina At Chapel Hill Androgen receptor proteins, recombinant DNA molecules coding for such, and use of such compositions
JPH0219363A (ja) 1988-07-06 1990-01-23 Fujisawa Pharmaceut Co Ltd イミダゾリジン誘導体
AU4005289A (en) 1988-08-25 1990-03-01 Smithkline Beecham Corporation Recombinant saccharomyces
US4938949A (en) 1988-09-12 1990-07-03 University Of New York Treatment of damaged bone marrow and dosage units therefor
DE3835168A1 (de) 1988-10-15 1990-04-19 Bayer Ag N-aryl-stickstoffheterocyclen, mehrere verfahren zu ihrer herstellung und ihre verwendung als herbizide
FR2646437B1 (fr) 1989-04-28 1991-08-30 Transgene Sa Nouvelles sequences d'adn, leur application en tant que sequence codant pour un peptide signal pour la secretion de proteines matures par des levures recombinantes, cassettes d'expression, levures transformees et procede de preparation de proteines correspondant
US5739136A (en) 1989-10-17 1998-04-14 Ellinwood, Jr.; Everett H. Intraoral dosing method of administering medicaments
FR2656302B1 (fr) 1989-12-22 1992-05-07 Roussel Uclaf Nouveau procede de preparation de l'anandron et derives de l'anandron.
US5017381A (en) 1990-05-02 1991-05-21 Alza Corporation Multi-unit pulsatile delivery system
FR2693461B1 (fr) * 1992-07-08 1994-09-02 Roussel Uclaf Nouvelles phénylimidazolidines substituées, leur procédé de préparation, leur application comme médicaments et les compositions pharmaceutiques les renfermant.
USRE35956E (en) 1991-01-09 1998-11-10 Roussel Uclaf Phenylimidazolidines having antiandrogenic activity
US5411981A (en) 1991-01-09 1995-05-02 Roussel Uclaf Phenylimidazolidines having antiandrogenic activity
FR2671348B1 (fr) 1991-01-09 1993-03-26 Roussel Uclaf Nouvelles phenylimidazolidines, leur procede de preparation, leur application comme medicaments et les compositions pharmaceutiques les renfermant.
US5229135A (en) 1991-11-22 1993-07-20 Prographarm Laboratories Sustained release diltiazem formulation
US5346913A (en) 1992-05-26 1994-09-13 Rohm And Haas Company N-iodopropargyl hydantoin compounds, compositions, preparation, and use as antimicrobial agents
US5323907A (en) 1992-06-23 1994-06-28 Multi-Comp, Inc. Child resistant package assembly for dispensing pharmaceutical medications
FR2694290B1 (fr) 1992-07-08 1994-09-02 Roussel Uclaf Nouvelles phénylimidazolidines éventuellement substituées, leur procédé de préparation, leur application comme médicaments et les compositions pharmaceutiques les renfermant.
TW521073B (en) 1994-01-05 2003-02-21 Hoechst Marion Roussel Inc New optionally substituted phenylimidazolidines, their preparation process, their use as anti-androgenic agent and the pharmaceutical compositions containing them
FR2715402B1 (fr) 1994-01-05 1996-10-04 Roussel Uclaf Nouvelles phénylimidazolines éventuellement substituées, leur procédé et des intermédiaires de préparation, leur application comme médicaments et les compositions pharmaceutiques les renfermant.
EP0748220A4 (fr) 1994-01-21 1997-09-10 Sepracor Inc Procedes et compositions de traitement de maladies dependantes des androgenes a l'aide de r-(-)-casodex optiquement pur
AU3086095A (en) 1994-07-29 1996-03-04 Suntory Limited Imidazolidine derivative and use thereof
FR2725206B1 (fr) 1994-09-29 1996-12-06 Roussel Uclaf Nouvelles imidazolidines substituees par un heterocycle, leur procede et des intermediaires de preparation, leur application comme medicaments et les compositions pharmaceutiques les renfermant
US5656651A (en) 1995-06-16 1997-08-12 Biophysica Inc. Androgenic directed compositions
DE19540027A1 (de) 1995-10-27 1997-04-30 Gruenenthal Gmbh Substituierte Imidazolidin-2,4-dion-Verbindungen als pharmazeutische Wirkstoffe
FR2741346B1 (fr) 1995-11-16 1997-12-19 Roussel Uclaf Nouveau procede de preparation de derives phenylimidazolidine
FR2741342B1 (fr) 1995-11-22 1998-02-06 Roussel Uclaf Nouvelles phenylimidazolidines fluorees ou hydroxylees, procede, intermediaires de preparation, application comme medicaments, nouvelle utilisation et compositions pharmaceutiques
WO1997019931A1 (fr) 1995-11-28 1997-06-05 American Home Products Corporation Derives de 2-(substitution sulfanyle)-3,5-dihydroimidazol-4-one
TW418195B (en) 1995-11-28 2001-01-11 American Home Prod 2-thioxo-imidazolidin-4-one derivatives
US5554607A (en) 1995-11-28 1996-09-10 American Home Products Corporation Use of 2-thioxo-imidazolin-4-one derivatives in the treatment of atherosclerosis
US5837284A (en) 1995-12-04 1998-11-17 Mehta; Atul M. Delivery of multiple doses of medications
FR2742749B1 (fr) 1995-12-22 1998-02-06 Roussel Uclaf Nouvelles phenylimidazolidines comportant notamment un radical nitrooxy ou carbonyloxy, procede et intermediaires de preparation, application comme medicaments, nouvelles utilisations et compositions pharmaceutiques
US6489163B1 (en) 1996-05-08 2002-12-03 Board Of Regents, The University Of Texas System Ribozyme mediated inactivation of the androgen receptor
US5726061A (en) 1996-10-08 1998-03-10 Smithkline Beechum Corporation Method of diagnosing and monitoring colorectal cancer
US7053263B2 (en) 1996-10-15 2006-05-30 The Regents Of The University Of California Mouse models of human prostate cancer progression
JP2001511146A (ja) 1997-02-03 2001-08-07 ダウ・アグロサイエンス・エル・エル・シー 殺菌・殺カビ剤としてのピリジン環上にカルボン酸誘導基を有する２−メトキシイミノ−２−（ピリジニルオキシメチル）フェニルアセトアミド
US5840329A (en) 1997-05-15 1998-11-24 Bioadvances Llc Pulsatile drug delivery system
US6506607B1 (en) 1997-12-24 2003-01-14 Millennium Pharmaceuticals, Inc. Methods and compositions for the identification and assessment of prostate cancer therapies and the diagnosis of prostate cancer
WO1999065494A1 (fr) 1998-06-15 1999-12-23 Merck & Co., Inc. Inhibiteurs de prenyl-proteine transferase
DE19940211A1 (de) 1998-09-22 2000-03-23 Degussa Verfahren zur Herstellung von Imidazolidin-2,4-dionen
US6673799B1 (en) 1998-09-22 2004-01-06 Yamanouchi Pharmaceutical Co. Ltd. Cyanophenyl derivative
AU1308400A (en) 1998-10-30 2000-05-22 G.D. Searle & Co. Novel amino acid heterocyclic amide derivatives useful as nitric oxide synthase inhibitors
US6472415B1 (en) 1998-12-18 2002-10-29 Biophysica, Inc. Androgen receptor suppressors in the therapy and diagnosis of prostate cancer, alopecia and other hyper-androgenic syndromes
WO2000044731A1 (fr) 1999-01-27 2000-08-03 G.D. Searle & Co. Nouveaux derives d'hydroamidino carboxylate utilise comme inhibiteurs de la synthase de l'oxyde nitrique
US6350763B1 (en) 1999-07-21 2002-02-26 Boehringer Ingelheim Pharmaceuticals, Inc. Small molecules useful in the treatment of inflammation disease
US6479063B2 (en) 1999-12-27 2002-11-12 Kenneth Weisman Therapeutic uses of hormonal manipulation using combinations of various agents to treat atherosclerosis
ES2284641T3 (es) 2000-05-31 2007-11-16 Tanabe Seiyaku Co., Ltd. Inhibidores de la adhesion celular mediada por alfa-l-beta-2.
US6482829B2 (en) 2000-06-08 2002-11-19 Hoffmann-La Roche Inc. Substituted heterocyclic siprodecane compound active as an antagonist of neurokinin 1 receptor
US20040077605A1 (en) 2001-06-20 2004-04-22 Salvati Mark E. Fused heterocyclic succinimide compounds and analogs thereof, modulators of nuclear hormone receptor function
WO2002053155A1 (fr) 2000-12-30 2002-07-11 Geron Corporation Inhibiteur de telomerase
FR2823209B1 (fr) 2001-04-04 2003-12-12 Fournier Lab Sa Nouvelles thiohydantoines et leur utilisation en therapeutique
US6710037B2 (en) 2001-05-01 2004-03-23 Schering Corporation Method of treating androgen-dependent disorders
BR0213025A (pt) 2001-10-01 2004-10-05 Bristol Myers Squibb Co Compostos de espiro-hidantoìna úteis como agentes antiinflamatórios
EP1453516A2 (fr) 2001-10-17 2004-09-08 Boehringer Ingelheim Pharma GmbH & Co.KG Nouvelles pyrimidines substituees, procede permettant de les produire et leur utilisation comme medicament
US6861432B2 (en) 2001-11-23 2005-03-01 Schering Aktiengesellschaft Piperazine derivatives that destabilize androgen receptors
GB0200283D0 (en) 2002-01-08 2002-02-20 Smithkline Beecham Plc Compounds
DE10218963A1 (de) 2002-04-27 2003-11-20 Aventis Pharma Gmbh Zubereitungen zur topischen Applikation von antiandrogen wirksamen Substanzen
TW200407324A (en) 2002-05-17 2004-05-16 Bristol Myers Squibb Co Bicyclic modulators of androgen receptor function
EP1576131A4 (fr) 2002-08-15 2008-08-13 Genzyme Corp Motifs d'expression de cellules endotheliales cerebrales
AU2002951247A0 (en) 2002-09-06 2002-09-19 Alchemia Limited Compounds that interact with kinases
FR2845384B1 (fr) 2002-10-04 2004-12-31 Fournier Lab Sa Composes derives de la 2-thiohydantoine et leur utilisation en therapeutique
CA2500977A1 (fr) 2002-10-04 2004-04-15 Laboratoires Fournier S.A. Composes derives de la 2-thiohydantoine et leur utilisation pour le traitement du diabete
FR2850652B1 (fr) 2003-01-31 2008-05-30 Aventis Pharma Sa Nouveaux derives d'uree cyclique, leur preparation et leur utilisation pharmaceutique comme inhibiteurs de kinases
JP2004252175A (ja) 2003-02-20 2004-09-09 Kyocera Mita Corp 現像装置、画像形成装置および現像剤の回収方法
RU2337908C2 (ru) 2003-06-12 2008-11-10 Ново Нордиск А/С Пиридинилкарбаматы в качестве ингибиторов гормон-чувствительной липазы
JP4664814B2 (ja) 2003-06-12 2011-04-06 中外製薬株式会社 イミダゾリジン誘導体
KR20060027338A (ko) 2003-06-12 2006-03-27 아스텔라스세이야쿠 가부시키가이샤 벤즈 아미드 유도체 또는 그 염
TW200523252A (en) 2003-10-31 2005-07-16 Takeda Pharmaceutical Pyridine compounds
US7256208B2 (en) 2003-11-13 2007-08-14 Bristol-Myers Squibb Company Monocyclic N-Aryl hydantoin modulators of androgen receptor function
EP1709152A4 (fr) 2003-12-15 2007-11-07 Univ California Signature moleculaire du suppresseur de tumeur pten
DE602004031881D1 (de) 2003-12-19 2011-04-28 Univ California Verfahren und materialien zur beurteilung von prostatakrebstherapien
US7718684B2 (en) 2004-02-24 2010-05-18 The Regents Of The University Of California Methods and materials for assessing prostate cancer therapies and compounds
EP1732543B1 (fr) 2004-03-15 2017-05-10 PTC Therapeutics, Inc. Derives de carboline tetra-cyclique utiles pour inhiber l'angiogenese
EP1621539A1 (fr) 2004-07-27 2006-02-01 Aventis Pharma S.A. Dérivées d'urée cyclique substitués par un heterocycle, leur prépration et leur utilisation pharmaceutique comee inhibiteurs de kinases
EP1775289B1 (fr) 2004-08-03 2011-03-30 Chugai Seiyaku Kabushiki Kaisha Nouveaux dérivés imidazolidine
AU2005280908A1 (en) 2004-09-09 2006-03-16 Chugai Seiyaku Kabushiki Kaisha Novel imidazolidine derivative and use thereof
EP3106162A1 (fr) 2005-05-13 2016-12-21 The Regents of the University of California Composes diarylhydantoines en tant qu'antagonistes du recepteur d'androgene pour le traitement du cancer
FR2889189A1 (fr) 2005-07-28 2007-02-02 Cerep Sa Composes derives d'hydantoine et leur utilistion en tant qu'antagonistes de mchr-1
GB0521373D0 (en) 2005-10-20 2005-11-30 Kudos Pharm Ltd Pthalazinone derivatives
CN101032486B (zh) 2006-03-08 2011-05-11 张宏 逆转唑类药物抗真菌活性多药耐药性的药用植物增效剂
CN101032483B (zh) * 2006-03-09 2011-05-04 陈德桂 调节雄激素受体活性的乙内酰脲衍生物及其应用
EP2656842B1 (fr) * 2006-03-27 2016-08-10 The Regents of The University of California Modulateur de récepteur androgène pour le traitement du cancer de la prostate et de maladies associées au récepteur androgène
WO2007127010A2 (fr) * 2006-03-29 2007-11-08 The Regents Of The University Of California Composés de diarylthiohydantoïne
US8461343B2 (en) * 2007-03-27 2013-06-11 Sloan-Kettering Institute For Cancer Research Synthesis of thiohydantoins
CA2966280A1 (fr) * 2007-10-26 2009-04-30 The Regents Of The University Of California Composes de diaryl-hydantoine
MX2011008858A (es) * 2009-02-24 2012-01-27 Medivation Prostate Therapeutics Inc Compuestos de diarilhidantoina y diariltiohidantoina especificos.
HUE037389T2 (hu) 2010-02-16 2018-08-28 Aragon Pharmaceuticals Inc Androgén receptor modulátorok és alkalmazásaik
ES2671343T3 (es) * 2010-02-24 2018-06-06 Medivation Prostate Therapeutics Llc Procesos para la síntesis de compuestos de diariltiohidantoína y diarilhidantoína
US20130253035A1 (en) 2010-08-16 2013-09-26 Duke University Camkk-beta as a target for treating cancer
CA2836277A1 (fr) 2011-05-17 2012-11-22 Takeda Pharmaceutical Company Limited Compositions pharmaceutiques et methodes de traitement du cancer
US20130045204A1 (en) 2011-08-19 2013-02-21 The University Of British Columbia Fluorinated bisphenol ether compounds and methods for their use
US20130079241A1 (en) 2011-09-15 2013-03-28 Jianhua Luo Methods for Diagnosing Prostate Cancer and Predicting Prostate Cancer Relapse
CA2856646C (fr) 2011-11-30 2020-01-14 Astrazeneca Ab Traitement combine du cancer
ES2836424T3 (es) 2012-09-26 2021-06-25 Aragon Pharmaceuticals Inc Antiandrógenos para tratar el cáncer de próstata no metastásico y resistente a la castración
CA3105575A1 (fr) 2013-01-15 2014-07-24 Aragon Pharmaceuticals, Inc. Modulateur du recepteur des androgenes et ses utilisations

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